Canonical Allele Identifier: CA1619114101
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31357054C= , CM000668.2:g.31357054C= GRCh38
NC_000006.11:g.31324831C= , CM000668.1:g.31324831C= GRCh37
NC_000006.10:g.31432810C= NCBI36
NG_023187.1:g.5159G=

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1546+32G=
ENST00000481849.6:n.1546+32G=
ENST00000497377.6:n.1546+32G=
ENST00000640094.2:c.73+32G= ENSP00000491275.2:n.73+32G=
ENST00000696558.1:c.73+32G= ENSP00000512716.1:n.73+32G=
ENST00000696559.1:c.73+32G= ENSP00000512717.1:n.73+32G=
ENST00000696560.1:c.73+32G= ENSP00000512718.1:n.73+32G=
ENST00000696561.1:c.73+32G= ENSP00000512719.1:n.73+32G=
ENST00000696562.1:c.73+32G= ENSP00000512720.1:n.73+32G=
ENST00000412585.7:c.73+32G= MANE Select ENSP00000399168.2:n.73+32G=
ENST00000412585.6:c.73+32G= ENSP00000399168.2:n.73+32G=
ENST00000434333.1:c.10G= ENSP00000405931.1:p.Ala4=
ENST00000498007.1:n.94+32G=
ENST00000603274.1:n.408C=
NM_005514.6:c.73+32G= NP_005505.2:n.73+32G=
XM_011514556.1:c.10G= XP_011512858.1:p.Ala4=
XM_011514557.1:c.73+32G= XP_011512859.1:n.73+32G=
XR_926175.1:n.83+32G=
NM_005514.7:c.73+32G= NP_005505.2:n.73+32G=
NM_005514.8:c.73+32G= MANE Select NP_005505.2:n.73+32G=