Canonical Allele Identifier: CA2677955099

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355205-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355206del , CM000668.2:g.31355206del	GRCh38
NC_000006.11:g.31322983del , CM000668.1:g.31322983del	GRCh37
NC_000006.10:g.31430962del	NCBI36
NG_023187.1:g.7007del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2960del
ENST00000481849.6:n.2479del
ENST00000497377.6:n.2386del
ENST00000640094.2:c.895+111del	ENSP00000491275.2:n.895+111del
ENST00000696558.1:c.982del	ENSP00000512716.1:n.982del
ENST00000696559.1:c.913del	ENSP00000512717.1:p.Thr305ProfsTer14
ENST00000696560.1:c.913del	ENSP00000512718.1:p.Thr305ProfsTer14
ENST00000696561.1:c.913del	ENSP00000512719.1:p.Thr305ProfsTer14
ENST00000696562.1:c.913del	ENSP00000512720.1:p.Thr305ProfsTer14
ENST00000412585.7:c.913del MANE Select	ENSP00000399168.2:p.Thr305ProfsTer14
ENST00000640094.1:c.88+111del	ENSP00000491275.1:n.88+111del
ENST00000412585.6:c.913del	ENSP00000399168.2:p.Thr305ProfsTer14
ENST00000463574.1:n.504del
NM_005514.6:c.913del	NP_005505.2:p.Thr305ProfsTer14
XM_011514556.1:c.946del	XP_011512858.1:p.Thr316ProfsTer14
XM_011514557.1:c.895+111del	XP_011512859.1:n.895+111del
XR_926175.1:n.1352del
NM_005514.7:c.913del	NP_005505.2:p.Thr305ProfsTer14
NM_005514.8:c.913del MANE Select	NP_005505.2:p.Thr305ProfsTer14