Canonical Allele Identifier: CA1619078739
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270002C= , CM000668.2:g.31270002C= GRCh38
NC_000006.11:g.31237779C= , CM000668.1:g.31237779C= GRCh37
NC_000006.10:g.31345758C= NCBI36
NG_029422.2:g.7130G=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.979G= MANE Select ENSP00000365402.5:p.Val327=
ENST00000376228.9:c.979G= ENSP00000365402.5:p.Val327=
ENST00000376237.8:c.*566G= ENSP00000365412.4:n.*566G=
ENST00000383329.7:c.979G= ENSP00000372819.3:p.Val327=
ENST00000470363.5:n.297G=
ENST00000487245.5:n.1338G=
NM_002117.5:c.979G= NP_002108.4:p.Val327=
NM_002117.6:c.979G= MANE Select NP_002108.4:p.Val327=