Canonical Allele Identifier: CA1619080826
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271708C= , CM000668.2:g.31271708C= GRCh38
NC_000006.11:g.31239485C= , CM000668.1:g.31239485C= GRCh37
NC_000006.10:g.31347464C= NCBI36
NG_029422.2:g.5424G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.234G= MANE Select ENSP00000365402.5:p.Gln78=
ENST00000376228.9:c.234G= ENSP00000365402.5:p.Gln78=
ENST00000376237.8:c.234G= ENSP00000365412.4:p.Gln78=
ENST00000383329.7:c.234G= ENSP00000372819.3:p.Gln78=
ENST00000415537.1:c.232G=
ENST00000484378.1:n.253G=
ENST00000487245.5:n.343G=
ENST00000495835.1:n.423G=
NM_002117.5:c.234G= NP_002108.4:p.Gln78=
NM_002117.6:c.234G= MANE Select NP_002108.4:p.Gln78=