Canonical Allele Identifier: CA1619080737
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271618G= , CM000668.2:g.31271618G= GRCh38
NC_000006.11:g.31239395G= , CM000668.1:g.31239395G= GRCh37
NC_000006.10:g.31347374G= NCBI36
NG_029422.2:g.5514C=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.324C= MANE Select ENSP00000365402.5:p.Tyr108=
ENST00000376228.9:c.324C= ENSP00000365402.5:p.Tyr108=
ENST00000376237.8:c.324C= ENSP00000365412.4:p.Tyr108=
ENST00000383329.7:c.324C= ENSP00000372819.3:p.Tyr108=
ENST00000415537.1:c.322C=
ENST00000484378.1:n.343C=
ENST00000487245.5:n.433C=
ENST00000495835.1:n.513C=
NM_002117.5:c.324C= NP_002108.4:p.Tyr108=
NM_002117.6:c.324C= MANE Select NP_002108.4:p.Tyr108=