Canonical Allele Identifier: CA372253706
Gene: TG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133133655C>G , CM000670.2:g.133133655C>G GRCh38
NC_000008.10:g.134145899C>G , CM000670.1:g.134145899C>G GRCh37
NC_000008.9:g.134215081C>G NCBI36
NG_015832.1:g.271695C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000220616.9:c.8183C>G MANE Select ENSP00000220616.4:p.Ser2728Cys
ENST00000220616.8:c.8183C>G ENSP00000220616.4:p.Ser2728Cys
ENST00000519178.5:c.3549C>G
ENST00000519543.5:c.2582C>G ENSP00000430430.1:p.Ser861Cys
ENST00000521107.1:c.395C>G ENSP00000430161.1:p.Ser132Cys
ENST00000522691.1:n.269C>G
ENST00000523756.5:c.4838C>G
NM_003235.4:c.8183C>G NP_003226.4:p.Ser2728Cys
XM_005251038.3:c.7991C>G XP_005251095.1:p.Ser2664Cys
XM_006716622.2:c.8120C>G XP_006716685.1:p.Ser2707Cys
XM_005251038.4:c.7991C>G XP_005251095.1:p.Ser2664Cys
XM_006716622.3:c.8120C>G XP_006716685.1:p.Ser2707Cys
XM_017013793.1:c.8117C>G XP_016869282.1:p.Ser2706Cys
XM_017013794.1:c.8048C>G XP_016869283.1:p.Ser2683Cys
XM_017013795.1:c.8012C>G XP_016869284.1:p.Ser2671Cys
XM_017013796.1:c.7964C>G XP_016869285.1:p.Ser2655Cys
XM_017013797.1:c.7922C>G XP_016869286.1:p.Ser2641Cys
NM_003235.5:c.8183C>G MANE Select NP_003226.4:p.Ser2728Cys