Canonical Allele Identifier: CA1619117433
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354603C= , CM000668.2:g.31354603C= GRCh38
NC_000006.11:g.31322380C= , CM000668.1:g.31322380C= GRCh37
NC_000006.10:g.31430359C= NCBI36
NG_023187.1:g.7610G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.3092+30G=
ENST00000481849.6:n.3052+30G=
ENST00000497377.6:n.2959+30G=
ENST00000640094.2:c.928+30G= ENSP00000491275.2:n.928+30G=
ENST00000696558.1:c.1114+30G= ENSP00000512716.1:n.1114+30G=
ENST00000696559.1:c.1045+30G= ENSP00000512717.1:n.1045+30G=
ENST00000696560.1:c.1045+30G= ENSP00000512718.1:n.1045+30G=
ENST00000696561.1:c.1045+30G= ENSP00000512719.1:n.1045+30G=
ENST00000696562.1:c.1045+30G= ENSP00000512720.1:n.1045+30G=
ENST00000412585.7:c.1045+30G= MANE Select ENSP00000399168.2:n.1045+30G=
ENST00000640094.1:c.121+30G= ENSP00000491275.1:n.121+30G=
ENST00000412585.6:c.1045+30G= ENSP00000399168.2:n.1045+30G=
ENST00000481849.5:n.204G=
ENST00000497377.5:n.444+30G=
NM_005514.6:c.1045+30G= NP_005505.2:n.1045+30G=
XM_011514556.1:c.1078+30G= XP_011512858.1:n.1078+30G=
XM_011514557.1:c.928+30G= XP_011512859.1:n.928+30G=
XR_926175.1:n.1484+30G=
NM_005514.7:c.1045+30G= NP_005505.2:n.1045+30G=
NM_005514.8:c.1045+30G= MANE Select NP_005505.2:n.1045+30G=