Canonical Allele Identifier: CA2580589238

Gene: GC

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71783222A>T , CM000666.2:g.71783222A>T	GRCh38
NC_000004.11:g.72648939A>T , CM000666.1:g.72648939A>T	GRCh37
NC_000004.10:g.72867803A>T	NCBI36
NG_012837.2:g.27299T>A
NG_012837.3:g.27299T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.58+739T>A MANE Select	ENSP00000273951.8:n.58+739T>A
ENST00000273951.12:c.58+739T>A	ENSP00000273951.8:n.58+739T>A
ENST00000504199.5:c.115+739T>A	ENSP00000421725.1:n.115+739T>A
ENST00000506245.1:c.58+739T>A	ENSP00000426718.1:n.58+739T>A
ENST00000509740.5:c.58+739T>A	ENSP00000422664.1:n.58+739T>A
ENST00000513476.5:c.58+739T>A	ENSP00000426683.1:n.58+739T>A
NM_000583.3:c.58+739T>A	NP_000574.2:n.58+739T>A
NM_001204306.1:c.58+739T>A	NP_001191235.1:n.58+739T>A
NM_001204307.1:c.115+739T>A	NP_001191236.1:n.115+739T>A
XM_006714177.2:c.58+739T>A	XP_006714240.1:n.58+739T>A
XM_006714177.3:c.58+739T>A	XP_006714240.1:n.58+739T>A
NM_000583.4:c.58+739T>A MANE Select	NP_000574.2:n.58+739T>A