Canonical Allele Identifier: CA372236919
Gene: TG HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000220616.9:c.6055G>T MANE Select ENSP00000220616.4:p.Gly2019Ter
ENST00000220616.8:c.6055G>T ENSP00000220616.4:p.Gly2019Ter
ENST00000519178.5:c.1421G>T
ENST00000519294.5:n.47G>T
ENST00000519543.5:c.517G>T ENSP00000430430.1:p.Gly173Ter
ENST00000520089.5:n.164G>T
ENST00000520197.5:n.192G>T
ENST00000523756.5:c.2710G>T
ENST00000524151.5:n.23G>T
NM_003235.4:c.6055G>T NP_003226.4:p.Gly2019Ter
XM_005251038.3:c.5863G>T XP_005251095.1:p.Gly1955Ter
XM_005251040.3:c.6055G>T XP_005251097.1:p.Gly2019Ter
XM_005251042.3:c.6055G>T XP_005251099.1:p.Gly2019Ter
XM_005251043.3:c.6055G>T XP_005251100.1:p.Gly2019Ter
XM_006716622.2:c.6055G>T XP_006716685.1:p.Gly2019Ter
XM_005251038.4:c.5863G>T XP_005251095.1:p.Gly1955Ter
XM_005251040.4:c.6055G>T XP_005251097.1:p.Gly2019Ter
XM_005251042.4:c.6055G>T XP_005251099.1:p.Gly2019Ter
XM_006716622.3:c.6055G>T XP_006716685.1:p.Gly2019Ter
XM_017013793.1:c.5989G>T XP_016869282.1:p.Gly1997Ter
XM_017013794.1:c.6055G>T XP_016869283.1:p.Gly2019Ter
XM_017013795.1:c.5884G>T XP_016869284.1:p.Gly1962Ter
XM_017013796.1:c.5836G>T XP_016869285.1:p.Gly1946Ter
XM_017013797.1:c.5794G>T XP_016869286.1:p.Gly1932Ter
XM_017013798.1:c.6055G>T XP_016869287.1:p.Gly2019Ter
XM_017013799.1:c.6055G>T XP_016869288.1:p.Gly2019Ter
XM_017013800.1:c.6055G>T XP_016869289.1:p.Gly2019Ter
NM_003235.5:c.6055G>T MANE Select NP_003226.4:p.Gly2019Ter