Canonical Allele Identifier: CA1619080480
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271282T= , CM000668.2:g.31271282T= GRCh38
NC_000006.11:g.31239059T= , CM000668.1:g.31239059T= GRCh37
NC_000006.10:g.31347038T= NCBI36
NG_029422.2:g.5850A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.410A= MANE Select ENSP00000365402.5:p.Tyr137=
ENST00000376228.9:c.410A= ENSP00000365402.5:p.Tyr137=
ENST00000376237.8:c.393A= ENSP00000365412.4:p.Val131=
ENST00000383329.7:c.410A= ENSP00000372819.3:p.Tyr137=
ENST00000415537.1:c.408A=
ENST00000484378.1:n.679A=
ENST00000487245.5:n.769A=
ENST00000495835.1:n.599A=
NM_002117.5:c.410A= NP_002108.4:p.Tyr137=
NM_002117.6:c.410A= MANE Select NP_002108.4:p.Tyr137=