Canonical Allele Identifier: CA2578564551

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355037-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355037C>A , CM000668.2:g.31355037C>A	GRCh38
NC_000006.11:g.31322814C>A , CM000668.1:g.31322814C>A	GRCh37
NC_000006.10:g.31430793C>A	NCBI36
NG_023187.1:g.7176G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.3059+70G>T
ENST00000481849.6:n.2648G>T
ENST00000497377.6:n.2555G>T
ENST00000640094.2:c.895+280G>T	ENSP00000491275.2:n.895+280G>T
ENST00000696558.1:c.1081+70G>T	ENSP00000512716.1:n.1081+70G>T
ENST00000696559.1:c.1012+70G>T	ENSP00000512717.1:n.1012+70G>T
ENST00000696560.1:c.1012+70G>T	ENSP00000512718.1:n.1012+70G>T
ENST00000696561.1:c.1012+70G>T	ENSP00000512719.1:n.1012+70G>T
ENST00000696562.1:c.1012+70G>T	ENSP00000512720.1:n.1012+70G>T
ENST00000412585.7:c.1012+70G>T MANE Select	ENSP00000399168.2:n.1012+70G>T
ENST00000640094.1:c.88+280G>T	ENSP00000491275.1:n.88+280G>T
ENST00000412585.6:c.1012+70G>T	ENSP00000399168.2:n.1012+70G>T
ENST00000497377.5:n.40G>T
NM_005514.6:c.1012+70G>T	NP_005505.2:n.1012+70G>T
XM_011514556.1:c.1045+70G>T	XP_011512858.1:n.1045+70G>T
XM_011514557.1:c.895+280G>T	XP_011512859.1:n.895+280G>T
XR_926175.1:n.1451+70G>T
NM_005514.7:c.1012+70G>T	NP_005505.2:n.1012+70G>T
NM_005514.8:c.1012+70G>T MANE Select	NP_005505.2:n.1012+70G>T