Canonical Allele Identifier: CA1467373900

Gene: GC

Linked Data

• dbSNP Id: rs1578290249

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71758327A>C , CM000666.2:g.71758327A>C	GRCh38
NC_000004.11:g.72624044A>C , CM000666.1:g.72624044A>C	GRCh37
NC_000004.10:g.72842908A>C	NCBI36
NG_012837.2:g.52194T>G
NG_012837.3:g.52194T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000273951.13:c.702-156T>G MANE Select	ENSP00000273951.8:n.702-156T>G
ENST00000273951.12:c.702-156T>G	ENSP00000273951.8:n.702-156T>G
ENST00000503472.5:n.586-156T>G
ENST00000504199.5:c.759-156T>G	ENSP00000421725.1:n.759-156T>G
ENST00000509740.5:c.702-156T>G	ENSP00000422664.1:n.702-156T>G
ENST00000513476.5:c.702-156T>G	ENSP00000426683.1:n.702-156T>G
NM_000583.3:c.702-156T>G	NP_000574.2:n.702-156T>G
NM_001204306.1:c.702-156T>G	NP_001191235.1:n.702-156T>G
NM_001204307.1:c.759-156T>G	NP_001191236.1:n.759-156T>G
XM_006714177.2:c.702-156T>G	XP_006714240.1:n.702-156T>G
XM_006714177.3:c.702-156T>G	XP_006714240.1:n.702-156T>G
NM_000583.4:c.702-156T>G MANE Select	NP_000574.2:n.702-156T>G