Canonical Allele Identifier: CA1467385649

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71784078G= , CM000666.2:g.71784078G=	GRCh38
NC_000004.11:g.72649795G= , CM000666.1:g.72649795G=	GRCh37
NC_000004.10:g.72868659G=	NCBI36
NG_012837.2:g.26443C=
NG_012837.3:g.26443C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.-60C= MANE Select	ENSP00000273951.8:n.-60C=
ENST00000273951.12:c.-60C=	ENSP00000273951.8:n.-60C=
ENST00000504199.5:c.22-24C=	ENSP00000421725.1:n.22-24C=
ENST00000506245.1:c.-36-24C=	ENSP00000426718.1:n.-36-24C=
NM_000583.3:c.-60C=	NP_000574.2:n.-60C=
NM_001204306.1:c.-36-24C=	NP_001191235.1:n.-36-24C=
NM_001204307.1:c.22-24C=	NP_001191236.1:n.22-24C=
XM_006714177.2:c.-60C=	XP_006714240.1:n.-60C=
XM_006714177.3:c.-60C=	XP_006714240.1:n.-60C=
NM_000583.4:c.-60C= MANE Select	NP_000574.2:n.-60C=