Canonical Allele Identifier: CA1087464774

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31355197-TG-T
• gnomAD v4: 6-31355197-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355201del , CM000668.2:g.31355201del	GRCh38
NC_000006.11:g.31322978del , CM000668.1:g.31322978del	GRCh37
NC_000006.10:g.31430957del	NCBI36
NG_023187.1:g.7015del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2968del
ENST00000481849.6:n.2487del
ENST00000497377.6:n.2394del
ENST00000640094.2:c.895+119del	ENSP00000491275.2:n.895+119del
ENST00000696558.1:c.990del	ENSP00000512716.1:n.990del
ENST00000696559.1:c.921del	ENSP00000512717.1:p.Ile308SerfsTer11
ENST00000696560.1:c.921del	ENSP00000512718.1:p.Ile308SerfsTer11
ENST00000696561.1:c.921del	ENSP00000512719.1:p.Ile308SerfsTer11
ENST00000696562.1:c.921del	ENSP00000512720.1:p.Ile308SerfsTer11
ENST00000412585.7:c.921del MANE Select	ENSP00000399168.2:p.Ile308SerfsTer11
ENST00000640094.1:c.88+119del	ENSP00000491275.1:n.88+119del
ENST00000412585.6:c.921del	ENSP00000399168.2:p.Ile308SerfsTer11
ENST00000463574.1:n.512del
NM_005514.6:c.921del	NP_005505.2:p.Ile308SerfsTer11
XM_011514556.1:c.954del	XP_011512858.1:p.Ile319SerfsTer11
XM_011514557.1:c.895+119del	XP_011512859.1:n.895+119del
XR_926175.1:n.1360del
NM_005514.7:c.921del	NP_005505.2:p.Ile308SerfsTer11
NM_005514.8:c.921del MANE Select	NP_005505.2:p.Ile308SerfsTer11