Canonical Allele Identifier: CA136836765
Gene: HLA-B HGNC NCBI

Linked Data

dbSNP Id: rs796742686

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357251_31357253delinsGAC , CM000668.2:g.31357251_31357253delinsGAC GRCh38
NC_000006.11:g.31325028_31325030delinsGAC , CM000668.1:g.31325028_31325030delinsGAC GRCh37
NC_000006.10:g.31433007_31433009delinsGAC NCBI36
NG_023187.1:g.4960_4962delinsGTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1379_1381delinsGTC
ENST00000481849.6:n.1379_1381delinsGTC
ENST00000497377.6:n.1379_1381delinsGTC
ENST00000696559.1:c.-95_-93delinsGTC ENSP00000512717.1:n.-95_-93delinsGTC
ENST00000696560.1:c.-95_-93delinsGTC ENSP00000512718.1:n.-95_-93delinsGTC
ENST00000696561.1:c.-95_-93delinsGTC ENSP00000512719.1:n.-95_-93delinsGTC
ENST00000696562.1:c.-95_-93delinsGTC ENSP00000512720.1:n.-95_-93delinsGTC
ENST00000603274.1:n.605_607delinsGAC