Canonical Allele Identifier: CA3710705
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs2308590
gnomAD v2: 6-31238942-G-C
gnomAD v3: 6-31271165-G-C
gnomAD v4: 6-31271165-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271165G>C , CM000668.2:g.31271165G>C GRCh38
NC_000006.11:g.31238942G>C , CM000668.1:g.31238942G>C GRCh37
NC_000006.10:g.31346921G>C NCBI36
NG_029422.2:g.5967C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.527C>G MANE Select ENSP00000365402.5:p.Ala176Gly
ENST00000376228.9:c.527C>G ENSP00000365402.5:p.Ala176Gly
ENST00000376237.8:c.*114C>G ENSP00000365412.4:n.*114C>G
ENST00000383329.7:c.527C>G ENSP00000372819.3:p.Ala176Gly
ENST00000415537.1:c.525C>G
ENST00000484378.1:n.796C>G
ENST00000487245.5:n.886C>G
ENST00000495835.1:n.716C>G
NM_002117.5:c.527C>G NP_002108.4:p.Ala176Gly
NM_002117.6:c.527C>G MANE Select NP_002108.4:p.Ala176Gly