Canonical Allele Identifier: CA2677958298

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357546-C-CAG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357546_31357547insAG , CM000668.2:g.31357546_31357547insAG	GRCh38
NC_000006.11:g.31325323_31325324insAG , CM000668.1:g.31325323_31325324insAG	GRCh37
NC_000006.10:g.31433302_31433303insAG	NCBI36
NG_023187.1:g.4666_4667insCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1338+67_1338+68insCT
ENST00000481849.6:n.1338+67_1338+68insCT
ENST00000497377.6:n.1338+67_1338+68insCT
ENST00000696559.1:c.-136+67_-136+68insCT	ENSP00000512717.1:n.-136+67_-136+68insCT
ENST00000696560.1:c.-136+67_-136+68insCT	ENSP00000512718.1:n.-136+67_-136+68insCT
ENST00000696561.1:c.-136+67_-136+68insCT	ENSP00000512719.1:n.-136+67_-136+68insCT
ENST00000696562.1:c.-135-254_-135-253insCT	ENSP00000512720.1:n.-135-254_-135-253insCT
ENST00000603274.1:n.900_901insAG
XR_926692.1:n.164+67_164+68insCT