Canonical Allele Identifier: CA136868012
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs281860449
gnomAD v3: 6-31271325-A-C
gnomAD v4: 6-31271325-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271325A>C , CM000668.2:g.31271325A>C GRCh38
NC_000006.11:g.31239102A>C , CM000668.1:g.31239102A>C GRCh37
NC_000006.10:g.31347081A>C NCBI36
NG_029422.2:g.5807T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.367T>G MANE Select ENSP00000365402.5:p.Ser123Ala
ENST00000376228.9:c.367T>G ENSP00000365402.5:p.Ser123Ala
ENST00000376237.8:c.350T>G ENSP00000365412.4:p.Val117Gly
ENST00000383329.7:c.367T>G ENSP00000372819.3:p.Ser123Ala
ENST00000415537.1:c.365T>G
ENST00000484378.1:n.636T>G
ENST00000487245.5:n.726T>G
ENST00000495835.1:n.556T>G
NM_002117.5:c.367T>G NP_002108.4:p.Ser123Ala
NM_002117.6:c.367T>G MANE Select NP_002108.4:p.Ser123Ala