Canonical Allele Identifier: CA1467385657

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71784089T= , CM000666.2:g.71784089T=	GRCh38
NC_000004.11:g.72649806T= , CM000666.1:g.72649806T=	GRCh37
NC_000004.10:g.72868670T=	NCBI36
NG_012837.2:g.26432A=
NG_012837.3:g.26432A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.12:c.-71A=	ENSP00000273951.8:n.-71A=
ENST00000504199.5:c.22-35A=	ENSP00000421725.1:n.22-35A=
ENST00000506245.1:c.-36-35A=	ENSP00000426718.1:n.-36-35A=
NM_000583.3:c.-71A=	NP_000574.2:n.-71A=
NM_001204306.1:c.-36-35A=	NP_001191235.1:n.-36-35A=
NM_001204307.1:c.22-35A=	NP_001191236.1:n.22-35A=
XM_006714177.2:c.-71A=	XP_006714240.1:n.-71A=