Canonical Allele Identifier: CA2677955055

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355157-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355158del , CM000668.2:g.31355158del	GRCh38
NC_000006.11:g.31322935del , CM000668.1:g.31322935del	GRCh37
NC_000006.10:g.31430914del	NCBI36
NG_023187.1:g.7055del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.3008del
ENST00000481849.6:n.2527del
ENST00000497377.6:n.2434del
ENST00000640094.2:c.895+159del	ENSP00000491275.2:n.895+159del
ENST00000696558.1:c.1030del	ENSP00000512716.1:n.1030del
ENST00000696559.1:c.961del	ENSP00000512717.1:p.Val321TrpfsTer10
ENST00000696560.1:c.961del	ENSP00000512718.1:p.Val321TrpfsTer10
ENST00000696561.1:c.961del	ENSP00000512719.1:p.Val321TrpfsTer10
ENST00000696562.1:c.961del	ENSP00000512720.1:p.Val321TrpfsTer10
ENST00000412585.7:c.961del MANE Select	ENSP00000399168.2:p.Val321TrpfsTer10
ENST00000640094.1:c.88+159del	ENSP00000491275.1:n.88+159del
ENST00000412585.6:c.961del	ENSP00000399168.2:p.Val321TrpfsTer10
ENST00000463574.1:n.552del
NM_005514.6:c.961del	NP_005505.2:p.Val321TrpfsTer10
XM_011514556.1:c.994del	XP_011512858.1:p.Val332TrpfsTer10
XM_011514557.1:c.895+159del	XP_011512859.1:n.895+159del
XR_926175.1:n.1400del
NM_005514.7:c.961del	NP_005505.2:p.Val321TrpfsTer10
NM_005514.8:c.961del MANE Select	NP_005505.2:p.Val321TrpfsTer10