Canonical Allele Identifier: CA2677948972
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31268802-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268802T>G , CM000668.2:g.31268802T>G GRCh38
NC_000006.11:g.31236579T>G , CM000668.1:g.31236579T>G GRCh37
NC_000006.10:g.31344558T>G NCBI36
NG_029422.2:g.8330A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*367A>C MANE Select ENSP00000365402.5:n.*367A>C
ENST00000376228.9:c.*367A>C ENSP00000365402.5:n.*367A>C
ENST00000376237.8:c.*1055A>C ENSP00000365412.4:n.*1055A>C
ENST00000383329.7:c.*367A>C ENSP00000372819.3:n.*367A>C
ENST00000466892.5:n.701A>C
ENST00000470363.5:n.1226A>C
ENST00000487245.5:n.1827A>C
NM_002117.5:c.*367A>C NP_002108.4:n.*367A>C
NM_002117.6:c.*367A>C MANE Select NP_002108.4:n.*367A>C