Canonical Allele Identifier: CA2677958299

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357546-C-CCCG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357547_31357548insCGC , CM000668.2:g.31357547_31357548insCGC	GRCh38
NC_000006.11:g.31325324_31325325insCGC , CM000668.1:g.31325324_31325325insCGC	GRCh37
NC_000006.10:g.31433303_31433304insCGC	NCBI36
NG_023187.1:g.4666_4667insCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1338+67_1338+68insCGG
ENST00000481849.6:n.1338+67_1338+68insCGG
ENST00000497377.6:n.1338+67_1338+68insCGG
ENST00000696559.1:c.-136+67_-136+68insCGG	ENSP00000512717.1:n.-136+67_-136+68insCGG
ENST00000696560.1:c.-136+67_-136+68insCGG	ENSP00000512718.1:n.-136+67_-136+68insCGG
ENST00000696561.1:c.-136+67_-136+68insCGG	ENSP00000512719.1:n.-136+67_-136+68insCGG
ENST00000696562.1:c.-135-254_-135-253insCGG	ENSP00000512720.1:n.-135-254_-135-253insCGG
ENST00000603274.1:n.901_902insCGC
XR_926692.1:n.164+67_164+68insCGG