Canonical Allele Identifier: CA4883951
Gene: TG HGNC NCBI

Linked Data

dbSNP Id: rs374714835

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.132908270C>T , CM000670.2:g.132908270C>T GRCh38
NC_000008.10:g.133920515C>T , CM000670.1:g.133920515C>T GRCh37
NC_000008.9:g.133989697C>T NCBI36
NG_015832.1:g.46311C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000220616.9:c.3932C>T MANE Select ENSP00000220616.4:p.Ala1311Val
ENST00000220616.8:c.3932C>T ENSP00000220616.4:p.Ala1311Val
ENST00000523756.5:c.587C>T
NM_003235.4:c.3932C>T NP_003226.4:p.Ala1311Val
XM_005251038.3:c.3932C>T XP_005251095.1:p.Ala1311Val
XM_005251040.3:c.3932C>T XP_005251097.1:p.Ala1311Val
XM_005251042.3:c.3932C>T XP_005251099.1:p.Ala1311Val
XM_005251043.3:c.3932C>T XP_005251100.1:p.Ala1311Val
XM_006716622.2:c.3932C>T XP_006716685.1:p.Ala1311Val
XM_005251038.4:c.3932C>T XP_005251095.1:p.Ala1311Val
XM_005251040.4:c.3932C>T XP_005251097.1:p.Ala1311Val
XM_005251042.4:c.3932C>T XP_005251099.1:p.Ala1311Val
XM_006716622.3:c.3932C>T XP_006716685.1:p.Ala1311Val
XM_017013793.1:c.3932C>T XP_016869282.1:p.Ala1311Val
XM_017013794.1:c.3932C>T XP_016869283.1:p.Ala1311Val
XM_017013795.1:c.3932C>T XP_016869284.1:p.Ala1311Val
XM_017013796.1:c.3932C>T XP_016869285.1:p.Ala1311Val
XM_017013797.1:c.3671C>T XP_016869286.1:p.Ala1224Val
XM_017013798.1:c.3932C>T XP_016869287.1:p.Ala1311Val
XM_017013799.1:c.3932C>T XP_016869288.1:p.Ala1311Val
XM_017013800.1:c.3932C>T XP_016869289.1:p.Ala1311Val
NM_003235.5:c.3932C>T MANE Select NP_003226.4:p.Ala1311Val