Canonical Allele Identifier: CA2677949310
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269057-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269057G>C , CM000668.2:g.31269057G>C GRCh38
NC_000006.11:g.31236834G>C , CM000668.1:g.31236834G>C GRCh37
NC_000006.10:g.31344813G>C NCBI36
NG_029422.2:g.8075C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*112C>G MANE Select ENSP00000365402.5:n.*112C>G
ENST00000376228.9:c.*112C>G ENSP00000365402.5:n.*112C>G
ENST00000376237.8:c.*800C>G ENSP00000365412.4:n.*800C>G
ENST00000383329.7:c.*112C>G ENSP00000372819.3:n.*112C>G
ENST00000466892.5:n.446C>G
ENST00000470363.5:n.971C>G
ENST00000487245.5:n.1572C>G
NM_002117.5:c.*112C>G NP_002108.4:n.*112C>G
NM_002117.6:c.*112C>G MANE Select NP_002108.4:n.*112C>G