Canonical Allele Identifier: CA2677955310

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355460-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355462del , CM000668.2:g.31355462del	GRCh38
NC_000006.11:g.31323239del , CM000668.1:g.31323239del	GRCh37
NC_000006.10:g.31431218del	NCBI36
NG_023187.1:g.6752del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2798del
ENST00000481849.6:n.2224del
ENST00000497377.6:n.2224del
ENST00000640094.2:c.751del	ENSP00000491275.2:p.Asp251ThrfsTer?
ENST00000696558.1:c.820del	ENSP00000512716.1:n.820del
ENST00000696559.1:c.751del	ENSP00000512717.1:p.Asp251ThrfsTer?
ENST00000696560.1:c.751del	ENSP00000512718.1:p.Asp251ThrfsTer?
ENST00000696561.1:c.751del	ENSP00000512719.1:p.Asp251ThrfsTer?
ENST00000696562.1:c.751del	ENSP00000512720.1:p.Asp251ThrfsTer?
ENST00000412585.7:c.751del MANE Select	ENSP00000399168.2:p.Asp251ThrfsTer?
ENST00000412585.6:c.751del	ENSP00000399168.2:p.Asp251ThrfsTer?
ENST00000463574.1:n.342del
ENST00000498007.1:n.1017del
NM_005514.6:c.751del	NP_005505.2:p.Asp251ThrfsTer?
XM_011514556.1:c.784del	XP_011512858.1:p.Asp262ThrfsTer?
XM_011514557.1:c.751del	XP_011512859.1:p.Asp251ThrfsTer?
XR_926175.1:n.1190del
NM_005514.7:c.751del	NP_005505.2:p.Asp251ThrfsTer?
NM_005514.8:c.751del MANE Select	NP_005505.2:p.Asp251ThrfsTer?