Canonical Allele Identifier: CA2677955095

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355201-GAC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355202_31355203del , CM000668.2:g.31355202_31355203del	GRCh38
NC_000006.11:g.31322979_31322980del , CM000668.1:g.31322979_31322980del	GRCh37
NC_000006.10:g.31430958_31430959del	NCBI36
NG_023187.1:g.7010_7011del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2963_2964del
ENST00000481849.6:n.2482_2483del
ENST00000497377.6:n.2389_2390del
ENST00000640094.2:c.895+114_895+115del	ENSP00000491275.2:n.895+114_895+115del
ENST00000696558.1:c.985_986del	ENSP00000512716.1:n.985_986del
ENST00000696559.1:c.916_917del	ENSP00000512717.1:p.Val306ProfsTer27
ENST00000696560.1:c.916_917del	ENSP00000512718.1:p.Val306ProfsTer27
ENST00000696561.1:c.916_917del	ENSP00000512719.1:p.Val306ProfsTer27
ENST00000696562.1:c.916_917del	ENSP00000512720.1:p.Val306ProfsTer27
ENST00000412585.7:c.916_917del MANE Select	ENSP00000399168.2:p.Val306ProfsTer27
ENST00000640094.1:c.88+114_88+115del	ENSP00000491275.1:n.88+114_88+115del
ENST00000412585.6:c.916_917del	ENSP00000399168.2:p.Val306ProfsTer27
ENST00000463574.1:n.507_508del
NM_005514.6:c.916_917del	NP_005505.2:p.Val306ProfsTer27
XM_011514556.1:c.949_950del	XP_011512858.1:p.Val317ProfsTer27
XM_011514557.1:c.895+114_895+115del	XP_011512859.1:n.895+114_895+115del
XR_926175.1:n.1355_1356del
NM_005514.7:c.916_917del	NP_005505.2:p.Val306ProfsTer27
NM_005514.8:c.916_917del MANE Select	NP_005505.2:p.Val306ProfsTer27