Canonical Allele Identifier: CA2677949379
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269090-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269090A>T , CM000668.2:g.31269090A>T GRCh38
NC_000006.11:g.31236867A>T , CM000668.1:g.31236867A>T GRCh37
NC_000006.10:g.31344846A>T NCBI36
NG_029422.2:g.8042T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*79T>A MANE Select ENSP00000365402.5:n.*79T>A
ENST00000376228.9:c.*79T>A ENSP00000365402.5:n.*79T>A
ENST00000376237.8:c.*767T>A ENSP00000365412.4:n.*767T>A
ENST00000383329.7:c.*79T>A ENSP00000372819.3:n.*79T>A
ENST00000466892.5:n.413T>A
ENST00000470363.5:n.938T>A
ENST00000487245.5:n.1539T>A
NM_002117.5:c.*79T>A NP_002108.4:n.*79T>A
NM_002117.6:c.*79T>A MANE Select NP_002108.4:n.*79T>A