Canonical Allele Identifier: CA449790551

Gene: HLA-B

Linked Data

• MyVariant Identifiers: chr6:g.31323143T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31355366T>A , CM000668.2:g.31355366T>A	GRCh38
NC_000006.11:g.31323143T>A , CM000668.1:g.31323143T>A	GRCh37
NC_000006.10:g.31431122T>A	NCBI36
NG_023187.1:g.6847A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000474381.2:n.2893A>T
ENST00000481849.6:n.2319A>T
ENST00000497377.6:n.2319A>T
ENST00000640094.2:c.846A>T	ENSP00000491275.2:p.Thr282=
ENST00000696558.1:c.915A>T	ENSP00000512716.1:n.915A>T
ENST00000696559.1:c.846A>T	ENSP00000512717.1:p.Thr282=
ENST00000696560.1:c.846A>T	ENSP00000512718.1:p.Thr282=
ENST00000696561.1:c.846A>T	ENSP00000512719.1:p.Thr282=
ENST00000696562.1:c.846A>T	ENSP00000512720.1:p.Thr282=
ENST00000412585.7:c.846A>T MANE Select	ENSP00000399168.2:p.Thr282=
ENST00000640094.1:c.39A>T	ENSP00000491275.1:p.Thr13=
ENST00000412585.6:c.846A>T	ENSP00000399168.2:p.Thr282=
ENST00000463574.1:n.437A>T
NM_005514.6:c.846A>T	NP_005505.2:p.Thr282=
XM_011514556.1:c.879A>T	XP_011512858.1:p.Thr293=
XM_011514557.1:c.846A>T	XP_011512859.1:p.Thr282=
XR_926175.1:n.1285A>T
NM_005514.7:c.846A>T	NP_005505.2:p.Thr282=
NM_005514.8:c.846A>T MANE Select	NP_005505.2:p.Thr282=