Canonical Allele Identifier: CA3710267
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs61759946
gnomAD v2: 6-31237159-C-G
gnomAD v3: 6-31269382-C-G
gnomAD v4: 6-31269382-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269382C>G , CM000668.2:g.31269382C>G GRCh38
NC_000006.11:g.31237159C>G , CM000668.1:g.31237159C>G GRCh37
NC_000006.10:g.31345138C>G NCBI36
NG_029422.2:g.7750G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1052G>C MANE Select ENSP00000365402.5:p.Ser351Thr
ENST00000376228.9:c.1052G>C ENSP00000365402.5:p.Ser351Thr
ENST00000376237.8:c.*639G>C ENSP00000365412.4:n.*639G>C
ENST00000383329.7:c.1070G>C ENSP00000372819.3:p.Ser357Thr
ENST00000466892.5:n.285G>C
ENST00000470363.5:n.810G>C
ENST00000487245.5:n.1411G>C
NM_002117.5:c.1052G>C NP_002108.4:p.Ser351Thr
NM_002117.6:c.1052G>C MANE Select NP_002108.4:p.Ser351Thr