Canonical Allele Identifier: CA1087445467

Gene: HLA-B

Linked Data

• dbSNP Id: rs1767248347
• gnomAD v3: 6-31357535-TGC-T
• gnomAD v4: 6-31357535-TGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357538_31357539del , CM000668.2:g.31357538_31357539del	GRCh38
NC_000006.11:g.31325315_31325316del , CM000668.1:g.31325315_31325316del	GRCh37
NC_000006.10:g.31433294_31433295del	NCBI36
NG_023187.1:g.4676_4677del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1338+77_1338+78del
ENST00000481849.6:n.1338+77_1338+78del
ENST00000497377.6:n.1338+77_1338+78del
ENST00000696559.1:c.-136+77_-136+78del	ENSP00000512717.1:n.-136+77_-136+78del
ENST00000696560.1:c.-136+77_-136+78del	ENSP00000512718.1:n.-136+77_-136+78del
ENST00000696561.1:c.-136+77_-136+78del	ENSP00000512719.1:n.-136+77_-136+78del
ENST00000696562.1:c.-135-244_-135-243del	ENSP00000512720.1:n.-135-244_-135-243del
ENST00000603274.1:n.892_893del
XR_926692.1:n.164+77_164+78del