Canonical Allele Identifier: CA2677956603

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356249-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356250dup , CM000668.2:g.31356250dup	GRCh38
NC_000006.11:g.31324027dup , CM000668.1:g.31324027dup	GRCh37
NC_000006.10:g.31432006dup	NCBI36
NG_023187.1:g.5963dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2009dup
ENST00000481849.6:n.2009dup
ENST00000497377.6:n.2009dup
ENST00000640094.2:c.536dup	ENSP00000491275.2:p.Arg180AlafsTer28
ENST00000696558.1:c.536dup	ENSP00000512716.1:p.Arg180AlafsTer28
ENST00000696559.1:c.536dup	ENSP00000512717.1:p.Arg180AlafsTer28
ENST00000696560.1:c.536dup	ENSP00000512718.1:p.Arg180AlafsTer28
ENST00000696561.1:c.536dup	ENSP00000512719.1:p.Arg180AlafsTer28
ENST00000696562.1:c.536dup	ENSP00000512720.1:p.Arg180AlafsTer28
ENST00000412585.7:c.536dup MANE Select	ENSP00000399168.2:p.Arg180AlafsTer28
ENST00000412585.6:c.536dup	ENSP00000399168.2:p.Arg180AlafsTer28
ENST00000434333.1:c.569dup	ENSP00000405931.1:p.Arg191AlafsTer28
ENST00000474381.1:n.411dup
ENST00000498007.1:n.802dup
NM_005514.6:c.536dup	NP_005505.2:p.Arg180AlafsTer28
XM_011514556.1:c.569dup	XP_011512858.1:p.Arg191AlafsTer28
XM_011514557.1:c.536dup	XP_011512859.1:p.Arg180AlafsTer28
XR_926175.1:n.546dup
NM_005514.7:c.536dup	NP_005505.2:p.Arg180AlafsTer28
NM_005514.8:c.536dup MANE Select	NP_005505.2:p.Arg180AlafsTer28