Canonical Allele Identifier: CA2677949289
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269045-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269045A>G , CM000668.2:g.31269045A>G GRCh38
NC_000006.11:g.31236822A>G , CM000668.1:g.31236822A>G GRCh37
NC_000006.10:g.31344801A>G NCBI36
NG_029422.2:g.8087T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*124T>C MANE Select ENSP00000365402.5:n.*124T>C
ENST00000376228.9:c.*124T>C ENSP00000365402.5:n.*124T>C
ENST00000376237.8:c.*812T>C ENSP00000365412.4:n.*812T>C
ENST00000383329.7:c.*124T>C ENSP00000372819.3:n.*124T>C
ENST00000466892.5:n.458T>C
ENST00000470363.5:n.983T>C
ENST00000487245.5:n.1584T>C
NM_002117.5:c.*124T>C NP_002108.4:n.*124T>C
NM_002117.6:c.*124T>C MANE Select NP_002108.4:n.*124T>C