Canonical Allele Identifier: CA186356750
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 2267294
ClinVar RCV Id: RCV002803987
dbSNP Id: rs867916302

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133133573A>G , CM000670.2:g.133133573A>G GRCh38
NC_000008.10:g.134145817A>G , CM000670.1:g.134145817A>G GRCh37
NC_000008.9:g.134214999A>G NCBI36
NG_015832.1:g.271613A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000220616.9:c.8101A>G MANE Select ENSP00000220616.4:p.Ser2701Gly
ENST00000220616.8:c.8101A>G ENSP00000220616.4:p.Ser2701Gly
ENST00000519178.5:c.3467A>G
ENST00000519543.5:c.2500A>G ENSP00000430430.1:p.Ser834Gly
ENST00000521107.1:c.313A>G ENSP00000430161.1:p.Ser105Gly
ENST00000522691.1:n.187A>G
ENST00000523756.5:c.4756A>G
NM_003235.4:c.8101A>G NP_003226.4:p.Ser2701Gly
XM_005251038.3:c.7909A>G XP_005251095.1:p.Ser2637Gly
XM_006716622.2:c.8038A>G XP_006716685.1:p.Ser2680Gly
XM_005251038.4:c.7909A>G XP_005251095.1:p.Ser2637Gly
XM_006716622.3:c.8038A>G XP_006716685.1:p.Ser2680Gly
XM_017013793.1:c.8035A>G XP_016869282.1:p.Ser2679Gly
XM_017013794.1:c.7966A>G XP_016869283.1:p.Ser2656Gly
XM_017013795.1:c.7930A>G XP_016869284.1:p.Ser2644Gly
XM_017013796.1:c.7882A>G XP_016869285.1:p.Ser2628Gly
XM_017013797.1:c.7840A>G XP_016869286.1:p.Ser2614Gly
NM_003235.5:c.8101A>G MANE Select NP_003226.4:p.Ser2701Gly