Canonical Allele Identifier: CA1467373914

Gene: GC

Linked Data

• dbSNP Id: rs1741855069

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71758367T>A , CM000666.2:g.71758367T>A	GRCh38
NC_000004.11:g.72624084T>A , CM000666.1:g.72624084T>A	GRCh37
NC_000004.10:g.72842948T>A	NCBI36
NG_012837.2:g.52154A>T
NG_012837.3:g.52154A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.702-196A>T MANE Select	ENSP00000273951.8:n.702-196A>T
ENST00000273951.12:c.702-196A>T	ENSP00000273951.8:n.702-196A>T
ENST00000503472.5:n.586-196A>T
ENST00000504199.5:c.759-196A>T	ENSP00000421725.1:n.759-196A>T
ENST00000509740.5:c.702-196A>T	ENSP00000422664.1:n.702-196A>T
ENST00000513476.5:c.702-196A>T	ENSP00000426683.1:n.702-196A>T
NM_000583.3:c.702-196A>T	NP_000574.2:n.702-196A>T
NM_001204306.1:c.702-196A>T	NP_001191235.1:n.702-196A>T
NM_001204307.1:c.759-196A>T	NP_001191236.1:n.759-196A>T
XM_006714177.2:c.702-196A>T	XP_006714240.1:n.702-196A>T
XM_006714177.3:c.702-196A>T	XP_006714240.1:n.702-196A>T
NM_000583.4:c.702-196A>T MANE Select	NP_000574.2:n.702-196A>T