Canonical Allele Identifier: CA1619118311
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355169A= , CM000668.2:g.31355169A= GRCh38
NC_000006.11:g.31322946A= , CM000668.1:g.31322946A= GRCh37
NC_000006.10:g.31430925A= NCBI36
NG_023187.1:g.7044T=

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.2997T=
ENST00000481849.6:n.2516T=
ENST00000497377.6:n.2423T=
ENST00000640094.2:c.895+148T= ENSP00000491275.2:n.895+148T=
ENST00000696558.1:c.1019T= ENSP00000512716.1:n.1019T=
ENST00000696559.1:c.950T= ENSP00000512717.1:p.Val317=
ENST00000696560.1:c.950T= ENSP00000512718.1:p.Val317=
ENST00000696561.1:c.950T= ENSP00000512719.1:p.Val317=
ENST00000696562.1:c.950T= ENSP00000512720.1:p.Val317=
ENST00000412585.7:c.950T= MANE Select ENSP00000399168.2:p.Val317=
ENST00000640094.1:c.88+148T= ENSP00000491275.1:n.88+148T=
ENST00000412585.6:c.950T= ENSP00000399168.2:p.Val317=
ENST00000463574.1:n.541T=
NM_005514.6:c.950T= NP_005505.2:p.Val317=
XM_011514556.1:c.983T= XP_011512858.1:p.Val328=
XM_011514557.1:c.895+148T= XP_011512859.1:n.895+148T=
XR_926175.1:n.1389T=
NM_005514.7:c.950T= NP_005505.2:p.Val317=
NM_005514.8:c.950T= MANE Select NP_005505.2:p.Val317=