Canonical Allele Identifier: CA4885898
Gene: TG HGNC NCBI

Linked Data

ClinVar Variation Id: 3176627
ClinVar RCV Id: RCV004474487
dbSNP Id: rs143950166

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.133133592G>A , CM000670.2:g.133133592G>A GRCh38
NC_000008.10:g.134145836G>A , CM000670.1:g.134145836G>A GRCh37
NC_000008.9:g.134215018G>A NCBI36
NG_015832.1:g.271632G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000220616.9:c.8120G>A MANE Select ENSP00000220616.4:p.Arg2707Gln
ENST00000220616.8:c.8120G>A ENSP00000220616.4:p.Arg2707Gln
ENST00000519178.5:c.3486G>A
ENST00000519543.5:c.2519G>A ENSP00000430430.1:p.Arg840Gln
ENST00000521107.1:c.332G>A ENSP00000430161.1:p.Arg111Gln
ENST00000522691.1:n.206G>A
ENST00000523756.5:c.4775G>A
NM_003235.4:c.8120G>A NP_003226.4:p.Arg2707Gln
XM_005251038.3:c.7928G>A XP_005251095.1:p.Arg2643Gln
XM_006716622.2:c.8057G>A XP_006716685.1:p.Arg2686Gln
XM_005251038.4:c.7928G>A XP_005251095.1:p.Arg2643Gln
XM_006716622.3:c.8057G>A XP_006716685.1:p.Arg2686Gln
XM_017013793.1:c.8054G>A XP_016869282.1:p.Arg2685Gln
XM_017013794.1:c.7985G>A XP_016869283.1:p.Arg2662Gln
XM_017013795.1:c.7949G>A XP_016869284.1:p.Arg2650Gln
XM_017013796.1:c.7901G>A XP_016869285.1:p.Arg2634Gln
XM_017013797.1:c.7859G>A XP_016869286.1:p.Arg2620Gln
NM_003235.5:c.8120G>A MANE Select NP_003226.4:p.Arg2707Gln