Canonical Allele Identifier: CA1619078768
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270013A= , CM000668.2:g.31270013A= GRCh38
NC_000006.11:g.31237790A= , CM000668.1:g.31237790A= GRCh37
NC_000006.10:g.31345769A= NCBI36
NG_029422.2:g.7119T=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.968T= MANE Select ENSP00000365402.5:p.Val323=
ENST00000376228.9:c.968T= ENSP00000365402.5:p.Val323=
ENST00000376237.8:c.*555T= ENSP00000365412.4:n.*555T=
ENST00000383329.7:c.968T= ENSP00000372819.3:p.Val323=
ENST00000470363.5:n.286T=
ENST00000487245.5:n.1327T=
NM_002117.5:c.968T= NP_002108.4:p.Val323=
NM_002117.6:c.968T= MANE Select NP_002108.4:p.Val323=