Canonical Allele Identifier: CA1087468025

Gene: HLA-B

Linked Data

• gnomAD v3: 6-31356375-ATG-A
• gnomAD v4: 6-31356375-ATG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356376_31356377del , CM000668.2:g.31356376_31356377del	GRCh38
NC_000006.11:g.31324153_31324154del , CM000668.1:g.31324153_31324154del	GRCh37
NC_000006.10:g.31432132_31432133del	NCBI36
NG_023187.1:g.5836_5837del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1882_1883del
ENST00000481849.6:n.1882_1883del
ENST00000497377.6:n.1882_1883del
ENST00000640094.2:c.409_410del	ENSP00000491275.2:p.His137Ter
ENST00000696558.1:c.409_410del	ENSP00000512716.1:p.His137Ter
ENST00000696559.1:c.409_410del	ENSP00000512717.1:p.His137Ter
ENST00000696560.1:c.409_410del	ENSP00000512718.1:p.His137Ter
ENST00000696561.1:c.409_410del	ENSP00000512719.1:p.His137Ter
ENST00000696562.1:c.409_410del	ENSP00000512720.1:p.His137Ter
ENST00000412585.7:c.409_410del MANE Select	ENSP00000399168.2:p.His137Ter
ENST00000412585.6:c.409_410del	ENSP00000399168.2:p.His137Ter
ENST00000434333.1:c.442_443del	ENSP00000405931.1:p.His148Ter
ENST00000474381.1:n.284_285del
ENST00000498007.1:n.675_676del
NM_005514.6:c.409_410del	NP_005505.2:p.His137Ter
XM_011514556.1:c.442_443del	XP_011512858.1:p.His148Ter
XM_011514557.1:c.409_410del	XP_011512859.1:p.His137Ter
XR_926175.1:n.419_420del
NM_005514.7:c.409_410del	NP_005505.2:p.His137Ter
NM_005514.8:c.409_410del MANE Select	NP_005505.2:p.His137Ter