Canonical Allele Identifier: CA1619117628
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354708G= , CM000668.2:g.31354708G= GRCh38
NC_000006.11:g.31322485G= , CM000668.1:g.31322485G= GRCh37
NC_000006.10:g.31430464G= NCBI36
NG_023187.1:g.7505C=

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.3060-43C=
ENST00000481849.6:n.2977C=
ENST00000497377.6:n.2884C=
ENST00000640094.2:c.896-43C= ENSP00000491275.2:n.896-43C=
ENST00000696558.1:c.1082-43C= ENSP00000512716.1:n.1082-43C=
ENST00000696559.1:c.1013-43C= ENSP00000512717.1:n.1013-43C=
ENST00000696560.1:c.1013-43C= ENSP00000512718.1:n.1013-43C=
ENST00000696561.1:c.1013-43C= ENSP00000512719.1:n.1013-43C=
ENST00000696562.1:c.1013-43C= ENSP00000512720.1:n.1013-43C=
ENST00000412585.7:c.1013-43C= MANE Select ENSP00000399168.2:n.1013-43C=
ENST00000640094.1:c.89-43C= ENSP00000491275.1:n.89-43C=
ENST00000412585.6:c.1013-43C= ENSP00000399168.2:n.1013-43C=
ENST00000481849.5:n.99C=
ENST00000497377.5:n.369C=
NM_005514.6:c.1013-43C= NP_005505.2:n.1013-43C=
XM_011514556.1:c.1046-43C= XP_011512858.1:n.1046-43C=
XM_011514557.1:c.896-43C= XP_011512859.1:n.896-43C=
XR_926175.1:n.1452-43C=
NM_005514.7:c.1013-43C= NP_005505.2:n.1013-43C=
NM_005514.8:c.1013-43C= MANE Select NP_005505.2:n.1013-43C=