Canonical Allele Identifier: CA449790549

Gene: HLA-B

Linked Data

• gnomAD v4: 6-31355363-G-A
• MyVariant Identifiers: chr6:g.31323140G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355363G>A , CM000668.2:g.31355363G>A	GRCh38
NC_000006.11:g.31323140G>A , CM000668.1:g.31323140G>A	GRCh37
NC_000006.10:g.31431119G>A	NCBI36
NG_023187.1:g.6850C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000474381.2:n.2896C>T
ENST00000481849.6:n.2322C>T
ENST00000497377.6:n.2322C>T
ENST00000640094.2:c.849C>T	ENSP00000491275.2:p.Cys283=
ENST00000696558.1:c.918C>T	ENSP00000512716.1:n.918C>T
ENST00000696559.1:c.849C>T	ENSP00000512717.1:p.Cys283=
ENST00000696560.1:c.849C>T	ENSP00000512718.1:p.Cys283=
ENST00000696561.1:c.849C>T	ENSP00000512719.1:p.Cys283=
ENST00000696562.1:c.849C>T	ENSP00000512720.1:p.Cys283=
ENST00000412585.7:c.849C>T MANE Select	ENSP00000399168.2:p.Cys283=
ENST00000640094.1:c.42C>T	ENSP00000491275.1:p.Cys14=
ENST00000412585.6:c.849C>T	ENSP00000399168.2:p.Cys283=
ENST00000463574.1:n.440C>T
NM_005514.6:c.849C>T	NP_005505.2:p.Cys283=
XM_011514556.1:c.882C>T	XP_011512858.1:p.Cys294=
XM_011514557.1:c.849C>T	XP_011512859.1:p.Cys283=
XR_926175.1:n.1288C>T
NM_005514.7:c.849C>T	NP_005505.2:p.Cys283=
NM_005514.8:c.849C>T MANE Select	NP_005505.2:p.Cys283=