Canonical Allele Identifier: CA798107023
Gene: GC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71751216T>C , CM000666.2:g.71751216T>C GRCh38
NC_000004.11:g.72616933T>C , CM000666.1:g.72616933T>C GRCh37
NC_000004.10:g.72835797T>C NCBI36
NG_012837.2:g.59305A>G
NG_012837.3:g.59305A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000273951.13:c.1395+1302A>G MANE Select ENSP00000273951.8:p.=
ENST00000273951.12:c.1395+1302A>G ENSP00000273951.8:p.=
ENST00000503364.5:n.68+3195A>G
ENST00000503472.5:n.1279+1302A>G
ENST00000504199.5:c.1452+1302A>G ENSP00000421725.1:p.=
ENST00000509740.5:c.*218+1302A>G ENSP00000422664.1:p.=
ENST00000513476.5:c.1395+1302A>G ENSP00000426683.1:p.=
NM_000583.3:c.1395+1302A>G NP_000574.2:p.=
NM_001204306.1:c.1395+1302A>G NP_001191235.1:p.=
NM_001204307.1:c.1452+1302A>G NP_001191236.1:p.=
XM_006714177.2:c.1262+3195A>G XP_006714240.1:p.=
XM_006714177.3:c.1262+3195A>G XP_006714240.1:p.=
NM_000583.4:c.1395+1302A>G MANE Select NP_000574.2:p.=