Canonical Allele Identifier: CA2677955108

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355214-GA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355216del , CM000668.2:g.31355216del	GRCh38
NC_000006.11:g.31322993del , CM000668.1:g.31322993del	GRCh37
NC_000006.10:g.31430972del	NCBI36
NG_023187.1:g.6998del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2951del
ENST00000481849.6:n.2470del
ENST00000497377.6:n.2377del
ENST00000640094.2:c.895+102del	ENSP00000491275.2:n.895+102del
ENST00000696558.1:c.973del	ENSP00000512716.1:n.973del
ENST00000696559.1:c.904del	ENSP00000512717.1:p.Ser302ProfsTer17
ENST00000696560.1:c.904del	ENSP00000512718.1:p.Ser302ProfsTer17
ENST00000696561.1:c.904del	ENSP00000512719.1:p.Ser302ProfsTer17
ENST00000696562.1:c.904del	ENSP00000512720.1:p.Ser302ProfsTer17
ENST00000412585.7:c.904del MANE Select	ENSP00000399168.2:p.Ser302ProfsTer17
ENST00000640094.1:c.88+102del	ENSP00000491275.1:n.88+102del
ENST00000412585.6:c.904del	ENSP00000399168.2:p.Ser302ProfsTer17
ENST00000463574.1:n.495del
NM_005514.6:c.904del	NP_005505.2:p.Ser302ProfsTer17
XM_011514556.1:c.937del	XP_011512858.1:p.Ser313ProfsTer17
XM_011514557.1:c.895+102del	XP_011512859.1:n.895+102del
XR_926175.1:n.1343del
NM_005514.7:c.904del	NP_005505.2:p.Ser302ProfsTer17
NM_005514.8:c.904del MANE Select	NP_005505.2:p.Ser302ProfsTer17