Canonical Allele Identifier: CA4885889

Gene: TG

Linked Data

• dbSNP Id: rs768009199
• ExAC: 8:134145796 G / A
• gnomAD v2: 8-134145796-G-A
• gnomAD v4: 8-133133552-G-A
• MyVariant Identifiers: chr8:g.134145796G>A (hg19) ; chr8:g.133133552G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133552G>A , CM000670.2:g.133133552G>A	GRCh38
NC_000008.10:g.134145796G>A , CM000670.1:g.134145796G>A	GRCh37
NC_000008.9:g.134214978G>A	NCBI36
NG_015832.1:g.271592G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8080G>A MANE Select	ENSP00000220616.4:p.Gly2694Arg
ENST00000220616.8:c.8080G>A	ENSP00000220616.4:p.Gly2694Arg
ENST00000519178.5:c.3446G>A
ENST00000519543.5:c.2479G>A	ENSP00000430430.1:p.Gly827Arg
ENST00000521107.1:c.292G>A	ENSP00000430161.1:p.Gly98Arg
ENST00000522691.1:n.166G>A
ENST00000523756.5:c.4735G>A
NM_003235.4:c.8080G>A	NP_003226.4:p.Gly2694Arg
XM_005251038.3:c.7888G>A	XP_005251095.1:p.Gly2630Arg
XM_006716622.2:c.8017G>A	XP_006716685.1:p.Gly2673Arg
XM_005251038.4:c.7888G>A	XP_005251095.1:p.Gly2630Arg
XM_006716622.3:c.8017G>A	XP_006716685.1:p.Gly2673Arg
XM_017013793.1:c.8014G>A	XP_016869282.1:p.Gly2672Arg
XM_017013794.1:c.7945G>A	XP_016869283.1:p.Gly2649Arg
XM_017013795.1:c.7909G>A	XP_016869284.1:p.Gly2637Arg
XM_017013796.1:c.7861G>A	XP_016869285.1:p.Gly2621Arg
XM_017013797.1:c.7819G>A	XP_016869286.1:p.Gly2607Arg
NM_003235.5:c.8080G>A MANE Select	NP_003226.4:p.Gly2694Arg