Canonical Allele Identifier: CA2509617931

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71773056C>A , CM000666.2:g.71773056C>A	GRCh38
NC_000004.11:g.72638773C>A , CM000666.1:g.72638773C>A	GRCh37
NC_000004.10:g.72857637C>A	NCBI36
NG_012837.2:g.37465G>T
NG_012837.3:g.37465G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.59-3656G>T MANE Select	ENSP00000273951.8:n.59-3656G>T
ENST00000273951.12:c.59-3656G>T	ENSP00000273951.8:n.59-3656G>T
ENST00000504199.5:c.116-3656G>T	ENSP00000421725.1:n.116-3656G>T
ENST00000506245.1:c.59-3656G>T	ENSP00000426718.1:n.59-3656G>T
ENST00000509740.5:c.59-3656G>T	ENSP00000422664.1:n.59-3656G>T
ENST00000513476.5:c.59-3656G>T	ENSP00000426683.1:n.59-3656G>T
NM_000583.3:c.59-3656G>T	NP_000574.2:n.59-3656G>T
NM_001204306.1:c.59-3656G>T	NP_001191235.1:n.59-3656G>T
NM_001204307.1:c.116-3656G>T	NP_001191236.1:n.116-3656G>T
XM_006714177.2:c.59-3656G>T	XP_006714240.1:n.59-3656G>T
XM_006714177.3:c.59-3656G>T	XP_006714240.1:n.59-3656G>T
NM_000583.4:c.59-3656G>T MANE Select	NP_000574.2:n.59-3656G>T