Canonical Allele Identifier: CA1619113212
Gene: HLA-B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31356797C= , CM000668.2:g.31356797C= GRCh38
NC_000006.11:g.31324574C= , CM000668.1:g.31324574C= GRCh37
NC_000006.10:g.31432553C= NCBI36
NG_023187.1:g.5416G=

Transcript Alleles

HGVS Amino-acid change
ENST00000474381.2:n.1707G=
ENST00000481849.6:n.1707G=
ENST00000497377.6:n.1707G=
ENST00000640094.2:c.234G= ENSP00000491275.2:p.Gln78=
ENST00000696558.1:c.234G= ENSP00000512716.1:p.Gln78=
ENST00000696559.1:c.234G= ENSP00000512717.1:p.Gln78=
ENST00000696560.1:c.234G= ENSP00000512718.1:p.Gln78=
ENST00000696561.1:c.234G= ENSP00000512719.1:p.Gln78=
ENST00000696562.1:c.234G= ENSP00000512720.1:p.Gln78=
ENST00000412585.7:c.234G= MANE Select ENSP00000399168.2:p.Gln78=
ENST00000412585.6:c.234G= ENSP00000399168.2:p.Gln78=
ENST00000434333.1:c.267G= ENSP00000405931.1:p.Gln89=
ENST00000474381.1:n.109G=
ENST00000498007.1:n.255G=
ENST00000603274.1:n.151C=
NM_005514.6:c.234G= NP_005505.2:p.Gln78=
XM_011514556.1:c.267G= XP_011512858.1:p.Gln89=
XM_011514557.1:c.234G= XP_011512859.1:p.Gln78=
XR_926175.1:n.244G=
NM_005514.7:c.234G= NP_005505.2:p.Gln78=
NM_005514.8:c.234G= MANE Select NP_005505.2:p.Gln78=