Canonical Allele Identifier: CA1619119527
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31355809G= , CM000668.2:g.31355809G= GRCh38
NC_000006.11:g.31323586G= , CM000668.1:g.31323586G= GRCh37
NC_000006.10:g.31431565G= NCBI36
NG_023187.1:g.6404C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.2450C=
ENST00000481849.6:n.2093-217C=
ENST00000497377.6:n.2093-217C=
ENST00000640094.2:c.620-217C= ENSP00000491275.2:n.620-217C=
ENST00000696558.1:c.620-3C= ENSP00000512716.1:n.620-3C=
ENST00000696559.1:c.620-217C= ENSP00000512717.1:n.620-217C=
ENST00000696560.1:c.620-217C= ENSP00000512718.1:n.620-217C=
ENST00000696561.1:c.620-217C= ENSP00000512719.1:n.620-217C=
ENST00000696562.1:c.620-217C= ENSP00000512720.1:n.620-217C=
ENST00000412585.7:c.620-217C= MANE Select ENSP00000399168.2:n.620-217C=
ENST00000412585.6:c.620-217C= ENSP00000399168.2:n.620-217C=
ENST00000434333.1:c.653-217C= ENSP00000405931.1:n.653-217C=
ENST00000474381.1:n.852C=
ENST00000498007.1:n.886-217C=
NM_005514.6:c.620-217C= NP_005505.2:n.620-217C=
XM_011514556.1:c.653-217C= XP_011512858.1:n.653-217C=
XM_011514557.1:c.620-217C= XP_011512859.1:n.620-217C=
XR_926175.1:n.987C=
NM_005514.7:c.620-217C= NP_005505.2:n.620-217C=
NM_005514.8:c.620-217C= MANE Select NP_005505.2:n.620-217C=