Canonical Allele Identifier: CA372236843
Gene: TG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132971861T>A , CM000670.2:g.132971861T>A GRCh38
NC_000008.10:g.133984106T>A , CM000670.1:g.133984106T>A GRCh37
NC_000008.9:g.134053288T>A NCBI36
NG_015832.1:g.109902T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000220616.9:c.6043T>A MANE Select ENSP00000220616.4:p.Ser2015Thr
ENST00000220616.8:c.6043T>A ENSP00000220616.4:p.Ser2015Thr
ENST00000519178.5:c.1409T>A
ENST00000519294.5:n.35T>A
ENST00000519543.5:c.505T>A ENSP00000430430.1:p.Ser169Thr
ENST00000520089.5:n.152T>A
ENST00000520197.5:n.180T>A
ENST00000523756.5:c.2698T>A
ENST00000524151.5:n.11T>A
NM_003235.4:c.6043T>A NP_003226.4:p.Ser2015Thr
XM_005251038.3:c.5851T>A XP_005251095.1:p.Ser1951Thr
XM_005251040.3:c.6043T>A XP_005251097.1:p.Ser2015Thr
XM_005251042.3:c.6043T>A XP_005251099.1:p.Ser2015Thr
XM_005251043.3:c.6043T>A XP_005251100.1:p.Ser2015Thr
XM_006716622.2:c.6043T>A XP_006716685.1:p.Ser2015Thr
XM_005251038.4:c.5851T>A XP_005251095.1:p.Ser1951Thr
XM_005251040.4:c.6043T>A XP_005251097.1:p.Ser2015Thr
XM_005251042.4:c.6043T>A XP_005251099.1:p.Ser2015Thr
XM_006716622.3:c.6043T>A XP_006716685.1:p.Ser2015Thr
XM_017013793.1:c.5977T>A XP_016869282.1:p.Ser1993Thr
XM_017013794.1:c.6043T>A XP_016869283.1:p.Ser2015Thr
XM_017013795.1:c.5872T>A XP_016869284.1:p.Ser1958Thr
XM_017013796.1:c.5824T>A XP_016869285.1:p.Ser1942Thr
XM_017013797.1:c.5782T>A XP_016869286.1:p.Ser1928Thr
XM_017013798.1:c.6043T>A XP_016869287.1:p.Ser2015Thr
XM_017013799.1:c.6043T>A XP_016869288.1:p.Ser2015Thr
XM_017013800.1:c.6043T>A XP_016869289.1:p.Ser2015Thr
NM_003235.5:c.6043T>A MANE Select NP_003226.4:p.Ser2015Thr