Canonical Allele Identifier: CA2677956541

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31356148-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356152dup , CM000668.2:g.31356152dup	GRCh38
NC_000006.11:g.31323929dup , CM000668.1:g.31323929dup	GRCh37
NC_000006.10:g.31431908dup	NCBI36
NG_023187.1:g.6064dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2110dup
ENST00000481849.6:n.2092+18dup
ENST00000497377.6:n.2092+18dup
ENST00000640094.2:c.619+18dup	ENSP00000491275.2:n.619+18dup
ENST00000696558.1:c.619+18dup	ENSP00000512716.1:n.619+18dup
ENST00000696559.1:c.619+18dup	ENSP00000512717.1:n.619+18dup
ENST00000696560.1:c.619+18dup	ENSP00000512718.1:n.619+18dup
ENST00000696561.1:c.619+18dup	ENSP00000512719.1:n.619+18dup
ENST00000696562.1:c.619+18dup	ENSP00000512720.1:n.619+18dup
ENST00000412585.7:c.619+18dup MANE Select	ENSP00000399168.2:n.619+18dup
ENST00000412585.6:c.619+18dup	ENSP00000399168.2:n.619+18dup
ENST00000434333.1:c.652+18dup	ENSP00000405931.1:n.652+18dup
ENST00000474381.1:n.512dup
ENST00000498007.1:n.885+18dup
NM_005514.6:c.619+18dup	NP_005505.2:n.619+18dup
XM_011514556.1:c.652+18dup	XP_011512858.1:n.652+18dup
XM_011514557.1:c.619+18dup	XP_011512859.1:n.619+18dup
XR_926175.1:n.647dup
NM_005514.7:c.619+18dup	NP_005505.2:n.619+18dup
NM_005514.8:c.619+18dup MANE Select	NP_005505.2:n.619+18dup