Canonical Allele Identifier: CA186295085

Gene: TG

Linked Data

• dbSNP Id: rs780979504
• gnomAD v4: 8-132971811-G-A
• COSMIC: COSM3942531
• MyVariant Identifiers: chr8:g.133984056G>A (hg19) ; chr8:g.132971811G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132971811G>A , CM000670.2:g.132971811G>A	GRCh38
NC_000008.10:g.133984056G>A , CM000670.1:g.133984056G>A	GRCh37
NC_000008.9:g.134053238G>A	NCBI36
NG_015832.1:g.109852G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.5993G>A MANE Select	ENSP00000220616.4:p.Arg1998Gln
ENST00000220616.8:c.5993G>A	ENSP00000220616.4:p.Arg1998Gln
ENST00000519178.5:c.1359G>A
ENST00000519543.5:c.455G>A	ENSP00000430430.1:p.Arg152Gln
ENST00000520089.5:n.102G>A
ENST00000520197.5:n.130G>A
ENST00000523756.5:c.2648G>A
NM_003235.4:c.5993G>A	NP_003226.4:p.Arg1998Gln
XM_005251038.3:c.5801G>A	XP_005251095.1:p.Arg1934Gln
XM_005251040.3:c.5993G>A	XP_005251097.1:p.Arg1998Gln
XM_005251042.3:c.5993G>A	XP_005251099.1:p.Arg1998Gln
XM_005251043.3:c.5993G>A	XP_005251100.1:p.Arg1998Gln
XM_006716622.2:c.5993G>A	XP_006716685.1:p.Arg1998Gln
XM_005251038.4:c.5801G>A	XP_005251095.1:p.Arg1934Gln
XM_005251040.4:c.5993G>A	XP_005251097.1:p.Arg1998Gln
XM_005251042.4:c.5993G>A	XP_005251099.1:p.Arg1998Gln
XM_006716622.3:c.5993G>A	XP_006716685.1:p.Arg1998Gln
XM_017013793.1:c.5927G>A	XP_016869282.1:p.Arg1976Gln
XM_017013794.1:c.5993G>A	XP_016869283.1:p.Arg1998Gln
XM_017013795.1:c.5822G>A	XP_016869284.1:p.Arg1941Gln
XM_017013796.1:c.5774G>A	XP_016869285.1:p.Arg1925Gln
XM_017013797.1:c.5732G>A	XP_016869286.1:p.Arg1911Gln
XM_017013798.1:c.5993G>A	XP_016869287.1:p.Arg1998Gln
XM_017013799.1:c.5993G>A	XP_016869288.1:p.Arg1998Gln
XM_017013800.1:c.5993G>A	XP_016869289.1:p.Arg1998Gln
NM_003235.5:c.5993G>A MANE Select	NP_003226.4:p.Arg1998Gln