Canonical Allele Identifier: CA2677955537

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355760-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355760G>T , CM000668.2:g.31355760G>T	GRCh38
NC_000006.11:g.31323537G>T , CM000668.1:g.31323537G>T	GRCh37
NC_000006.10:g.31431516G>T	NCBI36
NG_023187.1:g.6453C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2499C>A
ENST00000481849.6:n.2093-168C>A
ENST00000497377.6:n.2093-168C>A
ENST00000640094.2:c.620-168C>A	ENSP00000491275.2:n.620-168C>A
ENST00000696558.1:c.666C>A	ENSP00000512716.1:p.Ser222=
ENST00000696559.1:c.620-168C>A	ENSP00000512717.1:n.620-168C>A
ENST00000696560.1:c.620-168C>A	ENSP00000512718.1:n.620-168C>A
ENST00000696561.1:c.620-168C>A	ENSP00000512719.1:n.620-168C>A
ENST00000696562.1:c.620-168C>A	ENSP00000512720.1:n.620-168C>A
ENST00000412585.7:c.620-168C>A MANE Select	ENSP00000399168.2:n.620-168C>A
ENST00000412585.6:c.620-168C>A	ENSP00000399168.2:n.620-168C>A
ENST00000434333.1:c.653-168C>A	ENSP00000405931.1:n.653-168C>A
ENST00000463574.1:n.43C>A
ENST00000474381.1:n.901C>A
ENST00000498007.1:n.886-168C>A
NM_005514.6:c.620-168C>A	NP_005505.2:n.620-168C>A
XM_011514556.1:c.653-168C>A	XP_011512858.1:n.653-168C>A
XM_011514557.1:c.620-168C>A	XP_011512859.1:n.620-168C>A
XR_926175.1:n.1036C>A
NM_005514.7:c.620-168C>A	NP_005505.2:n.620-168C>A
NM_005514.8:c.620-168C>A MANE Select	NP_005505.2:n.620-168C>A