Canonical Allele Identifier: CA357199284

Gene: GC

Linked Data

• dbSNP Id: rs1311874616
• MyVariant Identifiers: chr4:g.72607578C>A (hg19) ; chr4:g.71741861C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.71741861C>A , CM000666.2:g.71741861C>A	GRCh38
NC_000004.11:g.72607578C>A , CM000666.1:g.72607578C>A	GRCh37
NC_000004.10:g.72826442C>A	NCBI36
NG_012837.2:g.68660G>T
NG_012837.3:g.68660G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000273951.13:c.*35G>T MANE Select	ENSP00000273951.8:n.*35G>T
ENST00000273951.12:c.*35G>T	ENSP00000273951.8:n.*35G>T
ENST00000503364.5:n.133G>T
ENST00000503472.5:n.1344G>T
ENST00000504199.5:c.*35G>T	ENSP00000421725.1:n.*35G>T
ENST00000509740.5:c.*283G>T	ENSP00000422664.1:n.*283G>T
ENST00000513476.5:c.1405G>T	ENSP00000426683.1:p.Gly469Ter
NM_000583.3:c.*35G>T	NP_000574.2:n.*35G>T
NM_001204306.1:c.*35G>T	NP_001191235.1:n.*35G>T
NM_001204307.1:c.*35G>T	NP_001191236.1:n.*35G>T
XM_006714177.2:c.*49G>T	XP_006714240.1:n.*49G>T
XM_006714177.3:c.*49G>T	XP_006714240.1:n.*49G>T
NM_000583.4:c.*35G>T MANE Select	NP_000574.2:n.*35G>T