Canonical Allele Identifier: CA372253479

Gene: TG

Linked Data

• dbSNP Id: rs1217648641
• gnomAD v2: 8-134145842-G-T
• gnomAD v4: 8-133133598-G-T
• MyVariant Identifiers: chr8:g.134145842G>T (hg19) ; chr8:g.133133598G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133598G>T , CM000670.2:g.133133598G>T	GRCh38
NC_000008.10:g.134145842G>T , CM000670.1:g.134145842G>T	GRCh37
NC_000008.9:g.134215024G>T	NCBI36
NG_015832.1:g.271638G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8126G>T MANE Select	ENSP00000220616.4:p.Gly2709Val
ENST00000220616.8:c.8126G>T	ENSP00000220616.4:p.Gly2709Val
ENST00000519178.5:c.3492G>T
ENST00000519543.5:c.2525G>T	ENSP00000430430.1:p.Gly842Val
ENST00000521107.1:c.338G>T	ENSP00000430161.1:p.Gly113Val
ENST00000522691.1:n.212G>T
ENST00000523756.5:c.4781G>T
NM_003235.4:c.8126G>T	NP_003226.4:p.Gly2709Val
XM_005251038.3:c.7934G>T	XP_005251095.1:p.Gly2645Val
XM_006716622.2:c.8063G>T	XP_006716685.1:p.Gly2688Val
XM_005251038.4:c.7934G>T	XP_005251095.1:p.Gly2645Val
XM_006716622.3:c.8063G>T	XP_006716685.1:p.Gly2688Val
XM_017013793.1:c.8060G>T	XP_016869282.1:p.Gly2687Val
XM_017013794.1:c.7991G>T	XP_016869283.1:p.Gly2664Val
XM_017013795.1:c.7955G>T	XP_016869284.1:p.Gly2652Val
XM_017013796.1:c.7907G>T	XP_016869285.1:p.Gly2636Val
XM_017013797.1:c.7865G>T	XP_016869286.1:p.Gly2622Val
NM_003235.5:c.8126G>T MANE Select	NP_003226.4:p.Gly2709Val