Canonical Allele Identifier: CA4883953
Gene: TG HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 258993
dbSNP Id: rs2069556

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132908273A>G , CM000670.2:g.132908273A>G GRCh38
NC_000008.10:g.133920518A>G , CM000670.1:g.133920518A>G GRCh37
NC_000008.9:g.133989700A>G NCBI36
NG_015832.1:g.46314A>G

Transcript Alleles

HGVS Amino-acid change
NM_003235.4:c.3935A>G VV NP_003226.4:p.Asp1312Gly
XM_005251038.3:c.3935A>G XP_005251095.1:p.Asp1312Gly
XM_005251040.3:c.3935A>G XP_005251097.1:p.Asp1312Gly
XM_005251042.3:c.3935A>G XP_005251099.1:p.Asp1312Gly
XM_005251043.3:c.3935A>G XP_005251100.1:p.Asp1312Gly
XM_006716622.2:c.3935A>G XP_006716685.1:p.Asp1312Gly
XM_005251038.4:c.3935A>G XP_005251095.1:p.Asp1312Gly
XM_005251040.4:c.3935A>G XP_005251097.1:p.Asp1312Gly
XM_005251042.4:c.3935A>G XP_005251099.1:p.Asp1312Gly
XM_006716622.3:c.3935A>G XP_006716685.1:p.Asp1312Gly
XM_017013793.1:c.3935A>G XP_016869282.1:p.Asp1312Gly
XM_017013794.1:c.3935A>G XP_016869283.1:p.Asp1312Gly
XM_017013795.1:c.3935A>G XP_016869284.1:p.Asp1312Gly
XM_017013796.1:c.3935A>G XP_016869285.1:p.Asp1312Gly
XM_017013797.1:c.3674A>G XP_016869286.1:p.Asp1225Gly
XM_017013798.1:c.3935A>G XP_016869287.1:p.Asp1312Gly
XM_017013799.1:c.3935A>G XP_016869288.1:p.Asp1312Gly
XM_017013800.1:c.3935A>G XP_016869289.1:p.Asp1312Gly
NM_003235.5:c.3935A>G VV MANE Preferred NP_003226.4:p.Asp1312Gly
ENST00000220616.8:c.3935A>G ENSP00000220616.4:p.Asp1312Gly
ENST00000523756.5:n.590A>G