Canonical Allele Identifier: CA2677956459

Gene: HLA-B

Linked Data

• dbSNP Id: rs772878053
• gnomAD v4: 6-31356116-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31356116A>T , CM000668.2:g.31356116A>T	GRCh38
NC_000006.11:g.31323893A>T , CM000668.1:g.31323893A>T	GRCh37
NC_000006.10:g.31431872A>T	NCBI36
NG_023187.1:g.6097T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2143T>A
ENST00000481849.6:n.2092+51T>A
ENST00000497377.6:n.2092+51T>A
ENST00000640094.2:c.619+51T>A	ENSP00000491275.2:n.619+51T>A
ENST00000696558.1:c.619+51T>A	ENSP00000512716.1:n.619+51T>A
ENST00000696559.1:c.619+51T>A	ENSP00000512717.1:n.619+51T>A
ENST00000696560.1:c.619+51T>A	ENSP00000512718.1:n.619+51T>A
ENST00000696561.1:c.619+51T>A	ENSP00000512719.1:n.619+51T>A
ENST00000696562.1:c.619+51T>A	ENSP00000512720.1:n.619+51T>A
ENST00000412585.7:c.619+51T>A MANE Select	ENSP00000399168.2:n.619+51T>A
ENST00000412585.6:c.619+51T>A	ENSP00000399168.2:n.619+51T>A
ENST00000434333.1:c.652+51T>A	ENSP00000405931.1:n.652+51T>A
ENST00000474381.1:n.545T>A
ENST00000498007.1:n.885+51T>A
NM_005514.6:c.619+51T>A	NP_005505.2:n.619+51T>A
XM_011514556.1:c.652+51T>A	XP_011512858.1:n.652+51T>A
XM_011514557.1:c.619+51T>A	XP_011512859.1:n.619+51T>A
XR_926175.1:n.680T>A
NM_005514.7:c.619+51T>A	NP_005505.2:n.619+51T>A
NM_005514.8:c.619+51T>A MANE Select	NP_005505.2:n.619+51T>A