Canonical Allele Identifier: CA2677957898

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31357112-G-GC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31357114dup , CM000668.2:g.31357114dup	GRCh38
NC_000006.11:g.31324891dup , CM000668.1:g.31324891dup	GRCh37
NC_000006.10:g.31432870dup	NCBI36
NG_023187.1:g.5100dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.1519dup
ENST00000481849.6:n.1519dup
ENST00000497377.6:n.1519dup
ENST00000640094.2:c.46dup	ENSP00000491275.2:p.Ala16GlyfsTer?
ENST00000696558.1:c.46dup	ENSP00000512716.1:p.Ala16GlyfsTer?
ENST00000696559.1:c.46dup	ENSP00000512717.1:p.Ala16GlyfsTer?
ENST00000696560.1:c.46dup	ENSP00000512718.1:p.Ala16GlyfsTer?
ENST00000696561.1:c.46dup	ENSP00000512719.1:p.Ala16GlyfsTer?
ENST00000696562.1:c.46dup	ENSP00000512720.1:p.Ala16GlyfsTer?
ENST00000412585.7:c.46dup MANE Select	ENSP00000399168.2:p.Ala16GlyfsTer?
ENST00000412585.6:c.46dup	ENSP00000399168.2:p.Ala16GlyfsTer?
ENST00000434333.1:c.-50dup	ENSP00000405931.1:n.-50dup
ENST00000498007.1:n.67dup
ENST00000603274.1:n.468dup
NM_005514.6:c.46dup	NP_005505.2:p.Ala16GlyfsTer?
XM_011514557.1:c.46dup	XP_011512859.1:p.Ala16GlyfsTer?
XR_926175.1:n.56dup
NM_005514.7:c.46dup	NP_005505.2:p.Ala16GlyfsTer?
NM_005514.8:c.46dup MANE Select	NP_005505.2:p.Ala16GlyfsTer?