Canonical Allele Identifier: CA1467386086

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71785126T= , CM000666.2:g.71785126T=	GRCh38
NC_000004.11:g.72650843T= , CM000666.1:g.72650843T=	GRCh37
NC_000004.10:g.72869707T=	NCBI36
NG_012837.2:g.25395A=
NG_012837.3:g.25395A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000504199.5:c.22-1072A=	ENSP00000421725.1:n.22-1072A=
ENST00000506245.1:c.-37+794A=	ENSP00000426718.1:n.-37+794A=
NM_001204306.1:c.-36-1072A=	NP_001191235.1:n.-36-1072A=
NM_001204307.1:c.22-1072A=	NP_001191236.1:n.22-1072A=