Canonical Allele Identifier: CA1619118701
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355344G= , CM000668.2:g.31355344G= GRCh38
NC_000006.11:g.31323121G= , CM000668.1:g.31323121G= GRCh37
NC_000006.10:g.31431100G= NCBI36
NG_023187.1:g.6869C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2915C=
ENST00000481849.6:n.2341C=
ENST00000497377.6:n.2341C=
ENST00000640094.2:c.868C= ENSP00000491275.2:p.Leu290=
ENST00000696558.1:c.937C= ENSP00000512716.1:n.937C=
ENST00000696559.1:c.868C= ENSP00000512717.1:p.Leu290=
ENST00000696560.1:c.868C= ENSP00000512718.1:p.Leu290=
ENST00000696561.1:c.868C= ENSP00000512719.1:p.Leu290=
ENST00000696562.1:c.868C= ENSP00000512720.1:p.Leu290=
ENST00000412585.7:c.868C= MANE Select ENSP00000399168.2:p.Leu290=
ENST00000640094.1:c.61C= ENSP00000491275.1:p.Leu21=
ENST00000412585.6:c.868C= ENSP00000399168.2:p.Leu290=
ENST00000463574.1:n.459C=
NM_005514.6:c.868C= NP_005505.2:p.Leu290=
XM_011514556.1:c.901C= XP_011512858.1:p.Leu301=
XM_011514557.1:c.868C= XP_011512859.1:p.Leu290=
XR_926175.1:n.1307C=
NM_005514.7:c.868C= NP_005505.2:p.Leu290=
NM_005514.8:c.868C= MANE Select NP_005505.2:p.Leu290=