Canonical Allele Identifier: CA1619117401
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31354592G= , CM000668.2:g.31354592G= GRCh38
NC_000006.11:g.31322369G= , CM000668.1:g.31322369G= GRCh37
NC_000006.10:g.31430348G= NCBI36
NG_023187.1:g.7621C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000474381.2:n.3092+41C=
ENST00000481849.6:n.3052+41C=
ENST00000497377.6:n.2959+41C=
ENST00000640094.2:c.928+41C= ENSP00000491275.2:n.928+41C=
ENST00000696558.1:c.1114+41C= ENSP00000512716.1:n.1114+41C=
ENST00000696559.1:c.1045+41C= ENSP00000512717.1:n.1045+41C=
ENST00000696560.1:c.1045+41C= ENSP00000512718.1:n.1045+41C=
ENST00000696561.1:c.1045+41C= ENSP00000512719.1:n.1045+41C=
ENST00000696562.1:c.1045+41C= ENSP00000512720.1:n.1045+41C=
ENST00000412585.7:c.1045+41C= MANE Select ENSP00000399168.2:n.1045+41C=
ENST00000640094.1:c.121+41C= ENSP00000491275.1:n.121+41C=
ENST00000412585.6:c.1045+41C= ENSP00000399168.2:n.1045+41C=
ENST00000481849.5:n.215C=
ENST00000497377.5:n.444+41C=
NM_005514.6:c.1045+41C= NP_005505.2:n.1045+41C=
XM_011514556.1:c.1078+41C= XP_011512858.1:n.1078+41C=
XM_011514557.1:c.928+41C= XP_011512859.1:n.928+41C=
XR_926175.1:n.1484+41C=
NM_005514.7:c.1045+41C= NP_005505.2:n.1045+41C=
NM_005514.8:c.1045+41C= MANE Select NP_005505.2:n.1045+41C=