Canonical Allele Identifier: CA1467385898

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71784656A= , CM000666.2:g.71784656A=	GRCh38
NC_000004.11:g.72650373A= , CM000666.1:g.72650373A=	GRCh37
NC_000004.10:g.72869237A=	NCBI36
NG_012837.2:g.25865T=
NG_012837.3:g.25865T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000504199.5:c.22-602T=	ENSP00000421725.1:n.22-602T=
ENST00000506245.1:c.-36-602T=	ENSP00000426718.1:n.-36-602T=
NM_001204306.1:c.-36-602T=	NP_001191235.1:n.-36-602T=
NM_001204307.1:c.22-602T=	NP_001191236.1:n.22-602T=