Canonical Allele Identifier: CA357205079
Gene: GC HGNC NCBI

Linked Data

gnomAD v4: 4-71756910-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71756910G>C , CM000666.2:g.71756910G>C GRCh38
NC_000004.11:g.72622627G>C , CM000666.1:g.72622627G>C GRCh37
NC_000004.10:g.72841491G>C NCBI36
NG_012837.2:g.53611C>G
NG_012837.3:g.53611C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000273951.13:c.836C>G MANE Select ENSP00000273951.8:p.Pro279Arg
ENST00000273951.12:c.836C>G ENSP00000273951.8:p.Pro279Arg
ENST00000503472.5:n.720C>G
ENST00000504199.5:c.893C>G ENSP00000421725.1:p.Pro298Arg
ENST00000509740.5:c.836C>G ENSP00000422664.1:p.Pro279Arg
ENST00000513476.5:c.836C>G ENSP00000426683.1:p.Pro279Arg
NM_000583.3:c.836C>G NP_000574.2:p.Pro279Arg
NM_001204306.1:c.836C>G NP_001191235.1:p.Pro279Arg
NM_001204307.1:c.893C>G NP_001191236.1:p.Pro298Arg
XM_006714177.2:c.836C>G XP_006714240.1:p.Pro279Arg
XM_006714177.3:c.836C>G XP_006714240.1:p.Pro279Arg
NM_000583.4:c.836C>G MANE Select NP_000574.2:p.Pro279Arg