Canonical Allele Identifier: CA2677955342

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355567-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355568del , CM000668.2:g.31355568del	GRCh38
NC_000006.11:g.31323345del , CM000668.1:g.31323345del	GRCh37
NC_000006.10:g.31431324del	NCBI36
NG_023187.1:g.6645del

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2691del
ENST00000481849.6:n.2117del
ENST00000497377.6:n.2117del
ENST00000640094.2:c.644del	ENSP00000491275.2:p.His215ProfsTer11
ENST00000696558.1:c.713del	ENSP00000512716.1:n.713del
ENST00000696559.1:c.644del	ENSP00000512717.1:p.His215ProfsTer11
ENST00000696560.1:c.644del	ENSP00000512718.1:p.His215ProfsTer11
ENST00000696561.1:c.644del	ENSP00000512719.1:p.His215ProfsTer11
ENST00000696562.1:c.644del	ENSP00000512720.1:p.His215ProfsTer11
ENST00000412585.7:c.644del MANE Select	ENSP00000399168.2:p.His215ProfsTer11
ENST00000412585.6:c.644del	ENSP00000399168.2:p.His215ProfsTer11
ENST00000434333.1:c.677del	ENSP00000405931.1:p.His226ProfsTer11
ENST00000463574.1:n.235del
ENST00000474381.1:n.1093del
ENST00000498007.1:n.910del
NM_005514.6:c.644del	NP_005505.2:p.His215ProfsTer11
XM_011514556.1:c.677del	XP_011512858.1:p.His226ProfsTer11
XM_011514557.1:c.644del	XP_011512859.1:p.His215ProfsTer11
XR_926175.1:n.1083del
NM_005514.7:c.644del	NP_005505.2:p.His215ProfsTer11
NM_005514.8:c.644del MANE Select	NP_005505.2:p.His215ProfsTer11