Canonical Allele Identifier: CA363310139
Gene: HLA-B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355347C>A , CM000668.2:g.31355347C>A GRCh38
NC_000006.11:g.31323124C>A , CM000668.1:g.31323124C>A GRCh37
NC_000006.10:g.31431103C>A NCBI36
NG_023187.1:g.6866G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2912G>T
ENST00000481849.6:n.2338G>T
ENST00000497377.6:n.2338G>T
ENST00000640094.2:c.865G>T ENSP00000491275.2:p.Gly289Trp
ENST00000696558.1:c.934G>T ENSP00000512716.1:n.934G>T
ENST00000696559.1:c.865G>T ENSP00000512717.1:p.Gly289Trp
ENST00000696560.1:c.865G>T ENSP00000512718.1:p.Gly289Trp
ENST00000696561.1:c.865G>T ENSP00000512719.1:p.Gly289Trp
ENST00000696562.1:c.865G>T ENSP00000512720.1:p.Gly289Trp
ENST00000412585.7:c.865G>T MANE Select ENSP00000399168.2:p.Gly289Trp
ENST00000640094.1:c.58G>T ENSP00000491275.1:p.Gly20Trp
ENST00000412585.6:c.865G>T ENSP00000399168.2:p.Gly289Trp
ENST00000463574.1:n.456G>T
NM_005514.6:c.865G>T NP_005505.2:p.Gly289Trp
XM_011514556.1:c.898G>T XP_011512858.1:p.Gly300Trp
XM_011514557.1:c.865G>T XP_011512859.1:p.Gly289Trp
XR_926175.1:n.1304G>T
NM_005514.7:c.865G>T NP_005505.2:p.Gly289Trp
NM_005514.8:c.865G>T MANE Select NP_005505.2:p.Gly289Trp