Canonical Allele Identifier: CA1619119143
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355572T= , CM000668.2:g.31355572T= GRCh38
NC_000006.11:g.31323349T= , CM000668.1:g.31323349T= GRCh37
NC_000006.10:g.31431328T= NCBI36
NG_023187.1:g.6641A=

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2687A=
ENST00000481849.6:n.2113A=
ENST00000497377.6:n.2113A=
ENST00000640094.2:c.640A= ENSP00000491275.2:p.Thr214=
ENST00000696558.1:c.709A= ENSP00000512716.1:n.709A=
ENST00000696559.1:c.640A= ENSP00000512717.1:p.Thr214=
ENST00000696560.1:c.640A= ENSP00000512718.1:p.Thr214=
ENST00000696561.1:c.640A= ENSP00000512719.1:p.Thr214=
ENST00000696562.1:c.640A= ENSP00000512720.1:p.Thr214=
ENST00000412585.7:c.640A= MANE Select ENSP00000399168.2:p.Thr214=
ENST00000412585.6:c.640A= ENSP00000399168.2:p.Thr214=
ENST00000434333.1:c.673A= ENSP00000405931.1:p.Thr225=
ENST00000463574.1:n.231A=
ENST00000474381.1:n.1089A=
ENST00000498007.1:n.906A=
NM_005514.6:c.640A= NP_005505.2:p.Thr214=
XM_011514556.1:c.673A= XP_011512858.1:p.Thr225=
XM_011514557.1:c.640A= XP_011512859.1:p.Thr214=
XR_926175.1:n.1079A=
NM_005514.7:c.640A= NP_005505.2:p.Thr214=
NM_005514.8:c.640A= MANE Select NP_005505.2:p.Thr214=