Canonical Allele Identifier: CA372253691

Gene: TG

Linked Data

• dbSNP Id: rs756744668
• gnomAD v2: 8-134145895-A-T
• gnomAD v4: 8-133133651-A-T
• MyVariant Identifiers: chr8:g.134145895A>T (hg19) ; chr8:g.133133651A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133651A>T , CM000670.2:g.133133651A>T	GRCh38
NC_000008.10:g.134145895A>T , CM000670.1:g.134145895A>T	GRCh37
NC_000008.9:g.134215077A>T	NCBI36
NG_015832.1:g.271691A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8179A>T MANE Select	ENSP00000220616.4:p.Thr2727Ser
ENST00000220616.8:c.8179A>T	ENSP00000220616.4:p.Thr2727Ser
ENST00000519178.5:c.3545A>T
ENST00000519543.5:c.2578A>T	ENSP00000430430.1:p.Thr860Ser
ENST00000521107.1:c.391A>T	ENSP00000430161.1:p.Thr131Ser
ENST00000522691.1:n.265A>T
ENST00000523756.5:c.4834A>T
NM_003235.4:c.8179A>T	NP_003226.4:p.Thr2727Ser
XM_005251038.3:c.7987A>T	XP_005251095.1:p.Thr2663Ser
XM_006716622.2:c.8116A>T	XP_006716685.1:p.Thr2706Ser
XM_005251038.4:c.7987A>T	XP_005251095.1:p.Thr2663Ser
XM_006716622.3:c.8116A>T	XP_006716685.1:p.Thr2706Ser
XM_017013793.1:c.8113A>T	XP_016869282.1:p.Thr2705Ser
XM_017013794.1:c.8044A>T	XP_016869283.1:p.Thr2682Ser
XM_017013795.1:c.8008A>T	XP_016869284.1:p.Thr2670Ser
XM_017013796.1:c.7960A>T	XP_016869285.1:p.Thr2654Ser
XM_017013797.1:c.7918A>T	XP_016869286.1:p.Thr2640Ser
NM_003235.5:c.8179A>T MANE Select	NP_003226.4:p.Thr2727Ser