Canonical Allele Identifier: CA136867595
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs45626438
gnomAD v4: 6-31271284-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271284C>G , CM000668.2:g.31271284C>G GRCh38
NC_000006.11:g.31239061C>G , CM000668.1:g.31239061C>G GRCh37
NC_000006.10:g.31347040C>G NCBI36
NG_029422.2:g.5848G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.408G>C MANE Select ENSP00000365402.5:p.Gly136=
ENST00000376228.9:c.408G>C ENSP00000365402.5:p.Gly136=
ENST00000376237.8:c.391G>C ENSP00000365412.4:p.Val131Leu
ENST00000383329.7:c.408G>C ENSP00000372819.3:p.Gly136=
ENST00000415537.1:c.406G>C
ENST00000484378.1:n.677G>C
ENST00000487245.5:n.767G>C
ENST00000495835.1:n.597G>C
NM_002117.5:c.408G>C NP_002108.4:p.Gly136=
NM_002117.6:c.408G>C MANE Select NP_002108.4:p.Gly136=