Canonical Allele Identifier: CA1619116418
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354032A= , CM000668.2:g.31354032A= GRCh38
NC_000006.11:g.31321809A= , CM000668.1:g.31321809A= GRCh37
NC_000006.10:g.31429788A= NCBI36
NG_023187.1:g.8181T=

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3405T=
ENST00000481849.6:n.3365T=
ENST00000497377.6:n.3272T=
ENST00000696558.1:c.1427T= ENSP00000512716.1:n.1427T=
ENST00000696559.1:c.*269T= ENSP00000512717.1:n.*269T=
ENST00000696560.1:c.*269T= ENSP00000512718.1:n.*269T=
ENST00000696561.1:c.*269T= ENSP00000512719.1:n.*269T=
ENST00000696562.1:c.*269T= ENSP00000512720.1:n.*269T=
ENST00000412585.7:c.*269T= MANE Select ENSP00000399168.2:n.*269T=
ENST00000412585.6:c.*269T= ENSP00000399168.2:n.*269T=
ENST00000481849.5:n.593T=
ENST00000497377.5:n.757T=
NM_005514.6:c.*269T= NP_005505.2:n.*269T=
XM_011514556.1:c.*269T= XP_011512858.1:n.*269T=
XM_011514557.1:c.*269T= XP_011512859.1:n.*269T=
XR_926175.1:n.1797T=
NM_005514.7:c.*269T= NP_005505.2:n.*269T=
NM_005514.8:c.*269T= MANE Select NP_005505.2:n.*269T=