Canonical Allele Identifier: CA2677949460
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269142-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269142C>T , CM000668.2:g.31269142C>T GRCh38
NC_000006.11:g.31236919C>T , CM000668.1:g.31236919C>T GRCh37
NC_000006.10:g.31344898C>T NCBI36
NG_029422.2:g.7990G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*27G>A MANE Select ENSP00000365402.5:n.*27G>A
ENST00000376228.9:c.*27G>A ENSP00000365402.5:n.*27G>A
ENST00000376237.8:c.*715G>A ENSP00000365412.4:n.*715G>A
ENST00000383329.7:c.*27G>A ENSP00000372819.3:n.*27G>A
ENST00000466892.5:n.361G>A
ENST00000470363.5:n.886G>A
ENST00000487245.5:n.1487G>A
NM_002117.5:c.*27G>A NP_002108.4:n.*27G>A
NM_002117.6:c.*27G>A MANE Select NP_002108.4:n.*27G>A