Canonical Allele Identifier: CA1619080618
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271445A= , CM000668.2:g.31271445A= GRCh38
NC_000006.11:g.31239222A= , CM000668.1:g.31239222A= GRCh37
NC_000006.10:g.31347201A= NCBI36
NG_029422.2:g.5687T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-97T= MANE Select ENSP00000365402.5:n.344-97T=
ENST00000376228.9:c.344-97T= ENSP00000365402.5:n.344-97T=
ENST00000376237.8:c.344-114T= ENSP00000365412.4:n.344-114T=
ENST00000383329.7:c.344-97T= ENSP00000372819.3:n.344-97T=
ENST00000415537.1:c.342-97T=
ENST00000484378.1:n.516T=
ENST00000487245.5:n.606T=
ENST00000495835.1:n.533-97T=
NM_002117.5:c.344-97T= NP_002108.4:n.344-97T=
NM_002117.6:c.344-97T= MANE Select NP_002108.4:n.344-97T=