Canonical Allele Identifier: CA372236917

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.133984118G>A (hg19) ; chr8:g.132971873G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132971873G>A , CM000670.2:g.132971873G>A	GRCh38
NC_000008.10:g.133984118G>A , CM000670.1:g.133984118G>A	GRCh37
NC_000008.9:g.134053300G>A	NCBI36
NG_015832.1:g.109914G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6055G>A MANE Select	ENSP00000220616.4:p.Gly2019Arg
ENST00000220616.8:c.6055G>A	ENSP00000220616.4:p.Gly2019Arg
ENST00000519178.5:c.1421G>A
ENST00000519294.5:n.47G>A
ENST00000519543.5:c.517G>A	ENSP00000430430.1:p.Gly173Arg
ENST00000520089.5:n.164G>A
ENST00000520197.5:n.192G>A
ENST00000523756.5:c.2710G>A
ENST00000524151.5:n.23G>A
NM_003235.4:c.6055G>A	NP_003226.4:p.Gly2019Arg
XM_005251038.3:c.5863G>A	XP_005251095.1:p.Gly1955Arg
XM_005251040.3:c.6055G>A	XP_005251097.1:p.Gly2019Arg
XM_005251042.3:c.6055G>A	XP_005251099.1:p.Gly2019Arg
XM_005251043.3:c.6055G>A	XP_005251100.1:p.Gly2019Arg
XM_006716622.2:c.6055G>A	XP_006716685.1:p.Gly2019Arg
XM_005251038.4:c.5863G>A	XP_005251095.1:p.Gly1955Arg
XM_005251040.4:c.6055G>A	XP_005251097.1:p.Gly2019Arg
XM_005251042.4:c.6055G>A	XP_005251099.1:p.Gly2019Arg
XM_006716622.3:c.6055G>A	XP_006716685.1:p.Gly2019Arg
XM_017013793.1:c.5989G>A	XP_016869282.1:p.Gly1997Arg
XM_017013794.1:c.6055G>A	XP_016869283.1:p.Gly2019Arg
XM_017013795.1:c.5884G>A	XP_016869284.1:p.Gly1962Arg
XM_017013796.1:c.5836G>A	XP_016869285.1:p.Gly1946Arg
XM_017013797.1:c.5794G>A	XP_016869286.1:p.Gly1932Arg
XM_017013798.1:c.6055G>A	XP_016869287.1:p.Gly2019Arg
XM_017013799.1:c.6055G>A	XP_016869288.1:p.Gly2019Arg
XM_017013800.1:c.6055G>A	XP_016869289.1:p.Gly2019Arg
NM_003235.5:c.6055G>A MANE Select	NP_003226.4:p.Gly2019Arg