Canonical Allele Identifier: CA1619079071
Gene: HLA-C HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270115T= , CM000668.2:g.31270115T= GRCh38
NC_000006.11:g.31237892T= , CM000668.1:g.31237892T= GRCh37
NC_000006.10:g.31345871T= NCBI36
NG_029422.2:g.7017A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.896-30A= MANE Select ENSP00000365402.5:n.896-30A=
ENST00000376228.9:c.896-30A= ENSP00000365402.5:n.896-30A=
ENST00000376237.8:c.*483-30A= ENSP00000365412.4:n.*483-30A=
ENST00000383329.7:c.896-30A= ENSP00000372819.3:n.896-30A=
ENST00000470363.5:n.214-30A=
ENST00000487245.5:n.1255-30A=
NM_002117.5:c.896-30A= NP_002108.4:n.896-30A=
NM_002117.6:c.896-30A= MANE Select NP_002108.4:n.896-30A=