Canonical Allele Identifier: CA1619079089
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270121C= , CM000668.2:g.31270121C= GRCh38
NC_000006.11:g.31237898C= , CM000668.1:g.31237898C= GRCh37
NC_000006.10:g.31345877C= NCBI36
NG_029422.2:g.7011G=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.896-36G= MANE Select ENSP00000365402.5:n.896-36G=
ENST00000376228.9:c.896-36G= ENSP00000365402.5:n.896-36G=
ENST00000376237.8:c.*483-36G= ENSP00000365412.4:n.*483-36G=
ENST00000383329.7:c.896-36G= ENSP00000372819.3:n.896-36G=
ENST00000470363.5:n.214-36G=
ENST00000487245.5:n.1255-36G=
NM_002117.5:c.896-36G= NP_002108.4:n.896-36G=
NM_002117.6:c.896-36G= MANE Select NP_002108.4:n.896-36G=