Canonical Allele Identifier: CA2677954991

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355137-CGACCACAGCTCCGAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355145_31355159del , CM000668.2:g.31355145_31355159del	GRCh38
NC_000006.11:g.31322922_31322936del , CM000668.1:g.31322922_31322936del	GRCh37
NC_000006.10:g.31430901_31430915del	NCBI36
NG_023187.1:g.7061_7075del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3014_3028del
ENST00000481849.6:n.2533_2547del
ENST00000497377.6:n.2440_2454del
ENST00000640094.2:c.895+165_895+179del	ENSP00000491275.2:n.895+165_895+179del
ENST00000696558.1:c.1036_1050del	ENSP00000512716.1:n.1036_1050del
ENST00000696559.1:c.967_981del	ENSP00000512717.1:p.Ile323_Val327del
ENST00000696560.1:c.967_981del	ENSP00000512718.1:p.Ile323_Val327del
ENST00000696561.1:c.967_981del	ENSP00000512719.1:p.Ile323_Val327del
ENST00000696562.1:c.967_981del	ENSP00000512720.1:p.Ile323_Val327del
ENST00000412585.7:c.967_981del MANE Select	ENSP00000399168.2:p.Ile323_Val327del
ENST00000640094.1:c.88+165_88+179del	ENSP00000491275.1:n.88+165_88+179del
ENST00000412585.6:c.967_981del	ENSP00000399168.2:p.Ile323_Val327del
ENST00000463574.1:n.558_572del
NM_005514.6:c.967_981del	NP_005505.2:p.Ile323_Val327del
XM_011514556.1:c.1000_1014del	XP_011512858.1:p.Ile334_Val338del
XM_011514557.1:c.895+165_895+179del	XP_011512859.1:n.895+165_895+179del
XR_926175.1:n.1406_1420del
NM_005514.7:c.967_981del	NP_005505.2:p.Ile323_Val327del
NM_005514.8:c.967_981del MANE Select	NP_005505.2:p.Ile323_Val327del