Canonical Allele Identifier: CA1619080521
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271325A= , CM000668.2:g.31271325A= GRCh38
NC_000006.11:g.31239102A= , CM000668.1:g.31239102A= GRCh37
NC_000006.10:g.31347081A= NCBI36
NG_029422.2:g.5807T=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.367T= MANE Select ENSP00000365402.5:p.Ser123=
ENST00000376228.9:c.367T= ENSP00000365402.5:p.Ser123=
ENST00000376237.8:c.350T= ENSP00000365412.4:p.Val117=
ENST00000383329.7:c.367T= ENSP00000372819.3:p.Ser123=
ENST00000415537.1:c.365T=
ENST00000484378.1:n.636T=
ENST00000487245.5:n.726T=
ENST00000495835.1:n.556T=
NM_002117.5:c.367T= NP_002108.4:p.Ser123=
NM_002117.6:c.367T= MANE Select NP_002108.4:p.Ser123=