Canonical Allele Identifier: CA2677958296
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357545_31357547del , CM000668.2:g.31357545_31357547del GRCh38
NC_000006.11:g.31325322_31325324del , CM000668.1:g.31325322_31325324del GRCh37
NC_000006.10:g.31433301_31433303del NCBI36
NG_023187.1:g.4667_4669del

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.1338+68_1338+70del
ENST00000481849.6:n.1338+68_1338+70del
ENST00000497377.6:n.1338+68_1338+70del
ENST00000696559.1:c.-136+68_-136+70del ENSP00000512717.1:n.-136+68_-136+70del
ENST00000696560.1:c.-136+68_-136+70del ENSP00000512718.1:n.-136+68_-136+70del
ENST00000696561.1:c.-136+68_-136+70del ENSP00000512719.1:n.-136+68_-136+70del
ENST00000696562.1:c.-135-253_-135-251del ENSP00000512720.1:n.-135-253_-135-251del
ENST00000603274.1:n.899_901del
XR_926692.1:n.164+68_164+70del