Canonical Allele Identifier: CA3710567
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1050326
gnomAD v2: 6-31238147-C-G
gnomAD v3: 6-31270370-C-G
gnomAD v4: 6-31270370-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270370C>G , CM000668.2:g.31270370C>G GRCh38
NC_000006.11:g.31238147C>G , CM000668.1:g.31238147C>G GRCh37
NC_000006.10:g.31346126C>G NCBI36
NG_029422.2:g.6762G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.735G>C MANE Select ENSP00000365402.5:p.Gly245=
ENST00000376228.9:c.735G>C ENSP00000365402.5:p.Gly245=
ENST00000376237.8:c.*322G>C ENSP00000365412.4:n.*322G>C
ENST00000383329.7:c.735G>C ENSP00000372819.3:p.Gly245=
ENST00000415537.1:c.665-39G>C
ENST00000470363.5:n.53G>C
ENST00000487245.5:n.1094G>C
ENST00000495835.1:n.924G>C
NM_002117.5:c.735G>C NP_002108.4:p.Gly245=
NM_002117.6:c.735G>C MANE Select NP_002108.4:p.Gly245=