Canonical Allele Identifier: CA2677956874

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356400-GGCCCCACGTCGCA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356404_31356416del , CM000668.2:g.31356404_31356416del	GRCh38
NC_000006.11:g.31324181_31324193del , CM000668.1:g.31324181_31324193del	GRCh37
NC_000006.10:g.31432160_31432172del	NCBI36
NG_023187.1:g.5800_5812del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.1846_1858del
ENST00000481849.6:n.1846_1858del
ENST00000497377.6:n.1846_1858del
ENST00000640094.2:c.373_385del	ENSP00000491275.2:p.Cys125ArgfsTer22
ENST00000696558.1:c.373_385del	ENSP00000512716.1:p.Cys125ArgfsTer22
ENST00000696559.1:c.373_385del	ENSP00000512717.1:p.Cys125ArgfsTer22
ENST00000696560.1:c.373_385del	ENSP00000512718.1:p.Cys125ArgfsTer22
ENST00000696561.1:c.373_385del	ENSP00000512719.1:p.Cys125ArgfsTer22
ENST00000696562.1:c.373_385del	ENSP00000512720.1:p.Cys125ArgfsTer22
ENST00000412585.7:c.373_385del MANE Select	ENSP00000399168.2:p.Cys125ArgfsTer22
ENST00000412585.6:c.373_385del	ENSP00000399168.2:p.Cys125ArgfsTer22
ENST00000434333.1:c.406_418del	ENSP00000405931.1:p.Cys136ArgfsTer22
ENST00000474381.1:n.248_260del
ENST00000498007.1:n.639_651del
NM_005514.6:c.373_385del	NP_005505.2:p.Cys125ArgfsTer22
XM_011514556.1:c.406_418del	XP_011512858.1:p.Cys136ArgfsTer22
XM_011514557.1:c.373_385del	XP_011512859.1:p.Cys125ArgfsTer22
XR_926175.1:n.383_395del
NM_005514.7:c.373_385del	NP_005505.2:p.Cys125ArgfsTer22
NM_005514.8:c.373_385del MANE Select	NP_005505.2:p.Cys125ArgfsTer22