Canonical Allele Identifier: CA1467373215

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71756818C= , CM000666.2:g.71756818C=	GRCh38
NC_000004.11:g.72622535C= , CM000666.1:g.72622535C=	GRCh37
NC_000004.10:g.72841399C=	NCBI36
NG_012837.2:g.53703G=
NG_012837.3:g.53703G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.928G= MANE Select	ENSP00000273951.8:p.Val310=
ENST00000273951.12:c.928G=	ENSP00000273951.8:p.Val310=
ENST00000503472.5:n.812G=
ENST00000504199.5:c.985G=	ENSP00000421725.1:p.Val329=
ENST00000509740.5:c.928G=	ENSP00000422664.1:p.Val310=
ENST00000513476.5:c.928G=	ENSP00000426683.1:p.Val310=
NM_000583.3:c.928G=	NP_000574.2:p.Val310=
NM_001204306.1:c.928G=	NP_001191235.1:p.Val310=
NM_001204307.1:c.985G=	NP_001191236.1:p.Val329=
XM_006714177.2:c.928G=	XP_006714240.1:p.Val310=
XM_006714177.3:c.928G=	XP_006714240.1:p.Val310=
NM_000583.4:c.928G= MANE Select	NP_000574.2:p.Val310=