Canonical Allele Identifier: CA2677949193
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31268968-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268968C>G , CM000668.2:g.31268968C>G GRCh38
NC_000006.11:g.31236745C>G , CM000668.1:g.31236745C>G GRCh37
NC_000006.10:g.31344724C>G NCBI36
NG_029422.2:g.8164G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*201G>C MANE Select ENSP00000365402.5:n.*201G>C
ENST00000376228.9:c.*201G>C ENSP00000365402.5:n.*201G>C
ENST00000376237.8:c.*889G>C ENSP00000365412.4:n.*889G>C
ENST00000383329.7:c.*201G>C ENSP00000372819.3:n.*201G>C
ENST00000466892.5:n.535G>C
ENST00000470363.5:n.1060G>C
ENST00000487245.5:n.1661G>C
NM_002117.5:c.*201G>C NP_002108.4:n.*201G>C
NM_002117.6:c.*201G>C MANE Select NP_002108.4:n.*201G>C