Canonical Allele Identifier: CA2677957920

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357139-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357143dup , CM000668.2:g.31357143dup	GRCh38
NC_000006.11:g.31324920dup , CM000668.1:g.31324920dup	GRCh37
NC_000006.10:g.31432899dup	NCBI36
NG_023187.1:g.5073dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1492dup
ENST00000481849.6:n.1492dup
ENST00000497377.6:n.1492dup
ENST00000640094.2:c.19dup	ENSP00000491275.2:p.Arg7ProfsTer?
ENST00000696558.1:c.19dup	ENSP00000512716.1:p.Arg7ProfsTer?
ENST00000696559.1:c.19dup	ENSP00000512717.1:p.Arg7ProfsTer?
ENST00000696560.1:c.19dup	ENSP00000512718.1:p.Arg7ProfsTer?
ENST00000696561.1:c.19dup	ENSP00000512719.1:p.Arg7ProfsTer?
ENST00000696562.1:c.19dup	ENSP00000512720.1:p.Arg7ProfsTer?
ENST00000412585.7:c.19dup MANE Select	ENSP00000399168.2:p.Arg7ProfsTer?
ENST00000412585.6:c.19dup	ENSP00000399168.2:p.Arg7ProfsTer?
ENST00000434333.1:c.-77dup	ENSP00000405931.1:n.-77dup
ENST00000498007.1:n.40dup
ENST00000603274.1:n.497dup
NM_005514.6:c.19dup	NP_005505.2:p.Arg7ProfsTer?
XM_011514557.1:c.19dup	XP_011512859.1:p.Arg7ProfsTer?
XR_926175.1:n.29dup
NM_005514.7:c.19dup	NP_005505.2:p.Arg7ProfsTer?
NM_005514.8:c.19dup MANE Select	NP_005505.2:p.Arg7ProfsTer?