Canonical Allele Identifier: CA1619119892

Gene: HLA-B

Linked Data

• dbSNP Id: rs1766926805
• gnomAD v3: 6-31356015-G-GGC
• gnomAD v4: 6-31356015-G-GGC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356016_31356017dup , CM000668.2:g.31356016_31356017dup	GRCh38
NC_000006.11:g.31323793_31323794dup , CM000668.1:g.31323793_31323794dup	GRCh37
NC_000006.10:g.31431772_31431773dup	NCBI36
NG_023187.1:g.6196_6197dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2242_2243dup
ENST00000481849.6:n.2092+150_2092+151dup
ENST00000497377.6:n.2092+150_2092+151dup
ENST00000640094.2:c.619+150_619+151dup	ENSP00000491275.2:n.619+150_619+151dup
ENST00000696558.1:c.619+150_619+151dup	ENSP00000512716.1:n.619+150_619+151dup
ENST00000696559.1:c.619+150_619+151dup	ENSP00000512717.1:n.619+150_619+151dup
ENST00000696560.1:c.619+150_619+151dup	ENSP00000512718.1:n.619+150_619+151dup
ENST00000696561.1:c.619+150_619+151dup	ENSP00000512719.1:n.619+150_619+151dup
ENST00000696562.1:c.619+150_619+151dup	ENSP00000512720.1:n.619+150_619+151dup
ENST00000412585.7:c.619+150_619+151dup MANE Select	ENSP00000399168.2:n.619+150_619+151dup
ENST00000412585.6:c.619+150_619+151dup	ENSP00000399168.2:n.619+150_619+151dup
ENST00000434333.1:c.652+150_652+151dup	ENSP00000405931.1:n.652+150_652+151dup
ENST00000474381.1:n.644_645dup
ENST00000498007.1:n.885+150_885+151dup
NM_005514.6:c.619+150_619+151dup	NP_005505.2:n.619+150_619+151dup
XM_011514556.1:c.652+150_652+151dup	XP_011512858.1:n.652+150_652+151dup
XM_011514557.1:c.619+150_619+151dup	XP_011512859.1:n.619+150_619+151dup
XR_926175.1:n.779_780dup
NM_005514.7:c.619+150_619+151dup	NP_005505.2:n.619+150_619+151dup
NM_005514.8:c.619+150_619+151dup MANE Select	NP_005505.2:n.619+150_619+151dup