HLA-Verify

Scan HLA typing report text, or model output about HLA, for allele-shaped tokens and classify each one: valid / legacy spelling such as A*0201 or Cw*0702 (valid, with modern form and flag deprecated_name) / G-P group / deleted (with successor) / fabricated / NMDP MAC code (seen, not expanded) / KIR name (out of scope, not checked); a valid token with fewer than four fields carries resolution, what

Normalize one reported HLA allele name (any era or reporting shorthand: legacy A*0101, Cw*0702 or Cw*07:02, G/P group names, A*02:XX, two-field A*02:01g, optional HLA- prefix) to current 2-field form, with G group, P group, serologic equivalent, and flags. NMDP MAC codes (A*02:AB) are recognised but not expanded (flag mac_code).

Look up one name in the pinned release and return what it is: assigned (G/P group, first release, confirmed status, WMDA serology, null flag), valid_prefix (member count and sample, plus resolution: what a name with fewer than four fields does and does not distinguish), group (a G or P group name: member count and sample), or deleted (successor). Reported shorthands are accepted as /v1/normalize a

Count a donor-recipient HLA match by the published counting rules (R1-R6): allele arithmetic over chromosomes, not a donor recommendation. recipient/donor: {"A": ["A*01:01","A*02:01"], "B": [...], ...} (two reported alleles per locus, any nomenclature era including G/P group names such as A*02:01:01G; allele strings only, no patient identifiers). framework: 6/6, 8/8, 10/10, 12/12, or antigen. Retu

QC-check one HLA typing (all loci) against the pinned release: resolves every reported allele, flags unresolvable/outdated/locus-mismatched/null alleles, flags too-many/single/homozygous per locus, computes the B-leader (-21 M/T) and KIR-ligand (C1/C2/Bw4) profile, and DRB3/4/5 expected-vs-reported. Nomenclature and internal-consistency checking of the report, not clinical interpretation. typing:

Donor/recipient immunogenetic compatibility under two published rule sets: HLA-B leader match (-21 M/T, Petersdorf 2020) for a single HLA-B mismatch, and KIR ligand (C1/C2/Bw4) class comparison, computed over each side's full typing QC. Rule checking against published frameworks; it does not rank or recommend a donor. recipient/donor: {"A": [...], "B": [...], "C": [...], "DRB1": [...], ...} (allel

Validate and normalize a GL String (Genotype List, ^ | + ~ / grammar): resolves every allele token, flags outdated/unresolvable names and structural problems (mixed loci within a slash-list, a repeated locus within a haplotype or across ^ blocks, more than two haplotypes, differing loci across a genotype or genotype list, empty elements), and returns the normalized string. Grammar and nomenclature

Which drugs an HLA typing carries a published pharmacogenomic association for. Looks each allele up in hla-pgx-open (CPIC guidelines + PharmGKB clinical annotations, CC BY-SA, snapshot date in every answer) after normalizing the name first, so any era or shorthand works (A*3101, B*5701, HLA-B*15:02:01G) and every conversion leaves a flag. Returns per allele the current name, the two-field form, th

For a donor-recipient pair, which genome carries each actionable HLA-drug association. Screens both typings as pgx_lookup does and marks every CPIC level-A, allele-positive association in_recipient, in_donor, discordant (present in exactly one) and whose_hla (both / recipient_only / donor_only). Guideline lookup over published CPIC and PharmGKB associations, keyed by two-field HLA allele. Decision

Translate HLA allele names from one IPD-IMGT/HLA release to another, through each allele's HLA ID, using the official Allelelist_history.txt (every release since 1.05.0). Give the names as they were written in release `from` (omit `from` to accept a name used in any release); `to` defaults to the current release. Each row says unchanged, renamed (to_name), deleted (reason, successor and its name i

Which HLA allele names were added, removed (with the deletion reason and successor) and renamed between two IPD-IMGT/HLA releases, optionally for one locus. Counts are complete; each list is cut at `limit` and `truncated` says so. Use it to see what a release update changes before re-running or re-reporting typings.

Every name the allele behind an HLA name has had, release by release since IPD-IMGT/HLA 1.05.0: its HLA ID, current name, the first and last release that used this name, the full timeline of names, and the deletion note if the name was retired. `as_of` adds what it was called in that release. Use it to answer when a name appeared, changed or disappeared. An allele string only, no patient identifie

Put a user on the free public beta's notification list for paid API keys. Ask before calling: it records the address they give you. Re-signing the same address is safe (status already_recorded). Someone who needs a higher rate limit today should email hello@hlaverify.com for a beta key instead of waiting.

Apply for free HLA-Verify access for an academic or nonprofit lab. Ask before calling: it records the address, institution and use case you give it. Approval is manual: a person reads every application, so it is not instant and not guaranteed. If it is approved the applicant is emailed a single-use code that takes 100% off a subscription for 12 months at self-serve checkout, with no card and no co

What this server is and is not, what to send it, benchmark evidence for why to use it, the beta state, and terms.