Canonical Allele Identifier: CA372253081
Gene: TG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133133498C>G , CM000670.2:g.133133498C>G GRCh38
NC_000008.10:g.134145742C>G , CM000670.1:g.134145742C>G GRCh37
NC_000008.9:g.134214924C>G NCBI36
NG_015832.1:g.271538C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000220616.9:c.8026C>G MANE Select ENSP00000220616.4:p.Arg2676Gly
ENST00000220616.8:c.8026C>G ENSP00000220616.4:p.Arg2676Gly
ENST00000519178.5:c.3392C>G
ENST00000519543.5:c.2425C>G ENSP00000430430.1:p.Arg809Gly
ENST00000521107.1:c.238C>G ENSP00000430161.1:p.Arg80Gly
ENST00000522691.1:n.112C>G
ENST00000523756.5:c.4681C>G
NM_003235.4:c.8026C>G NP_003226.4:p.Arg2676Gly
XM_005251038.3:c.7834C>G XP_005251095.1:p.Arg2612Gly
XM_006716622.2:c.7963C>G XP_006716685.1:p.Arg2655Gly
XM_005251038.4:c.7834C>G XP_005251095.1:p.Arg2612Gly
XM_006716622.3:c.7963C>G XP_006716685.1:p.Arg2655Gly
XM_017013793.1:c.7960C>G XP_016869282.1:p.Arg2654Gly
XM_017013794.1:c.7891C>G XP_016869283.1:p.Arg2631Gly
XM_017013795.1:c.7855C>G XP_016869284.1:p.Arg2619Gly
XM_017013796.1:c.7807C>G XP_016869285.1:p.Arg2603Gly
XM_017013797.1:c.7765C>G XP_016869286.1:p.Arg2589Gly
NM_003235.5:c.8026C>G MANE Select NP_003226.4:p.Arg2676Gly