Canonical Allele Identifier: CA15360575
Gene: GC HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3755967

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.71743681C>T , CM000666.2:g.71743681C>T GRCh38
NC_000004.11:g.72609398C>T , CM000666.1:g.72609398C>T GRCh37
NC_000004.10:g.72828262C>T NCBI36
NG_012837.2:g.66840G>A
NG_012837.3:g.66840G>A

Transcript Alleles

HGVS Amino-acid change
NM_000583.3:c.*26-1811G>A VV NP_000574.2:p.=
NM_001204306.1:c.*26-1811G>A VV NP_001191235.1:p.=
NM_001204307.1:c.*26-1811G>A VV NP_001191236.1:p.=
XM_006714177.2:c.*40-1811G>A XP_006714240.1:p.=
XM_006714177.3:c.*40-1811G>A XP_006714240.1:p.=
NM_000583.4:c.*26-1811G>A VV MANE Preferred NP_000574.2:p.=
ENST00000273951.12:c.*26-1811G>A ENSP00000273951.8:p.=
ENST00000503364.5:n.124-1811G>A
ENST00000503472.5:n.1335-1811G>A
ENST00000504199.5:c.*26-1811G>A ENSP00000421725.1:p.=
ENST00000509740.5:c.*274-1811G>A ENSP00000422664.1:p.=
ENST00000513476.5:c.1396-1811G>A ENSP00000426683.1:p.=