Canonical Allele Identifier: CA372253125

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145754A>G (hg19) ; chr8:g.133133510A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133510A>G , CM000670.2:g.133133510A>G	GRCh38
NC_000008.10:g.134145754A>G , CM000670.1:g.134145754A>G	GRCh37
NC_000008.9:g.134214936A>G	NCBI36
NG_015832.1:g.271550A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8038A>G MANE Select	ENSP00000220616.4:p.Thr2680Ala
ENST00000220616.8:c.8038A>G	ENSP00000220616.4:p.Thr2680Ala
ENST00000519178.5:c.3404A>G
ENST00000519543.5:c.2437A>G	ENSP00000430430.1:p.Thr813Ala
ENST00000521107.1:c.250A>G	ENSP00000430161.1:p.Thr84Ala
ENST00000522691.1:n.124A>G
ENST00000523756.5:c.4693A>G
NM_003235.4:c.8038A>G	NP_003226.4:p.Thr2680Ala
XM_005251038.3:c.7846A>G	XP_005251095.1:p.Thr2616Ala
XM_006716622.2:c.7975A>G	XP_006716685.1:p.Thr2659Ala
XM_005251038.4:c.7846A>G	XP_005251095.1:p.Thr2616Ala
XM_006716622.3:c.7975A>G	XP_006716685.1:p.Thr2659Ala
XM_017013793.1:c.7972A>G	XP_016869282.1:p.Thr2658Ala
XM_017013794.1:c.7903A>G	XP_016869283.1:p.Thr2635Ala
XM_017013795.1:c.7867A>G	XP_016869284.1:p.Thr2623Ala
XM_017013796.1:c.7819A>G	XP_016869285.1:p.Thr2607Ala
XM_017013797.1:c.7777A>G	XP_016869286.1:p.Thr2593Ala
NM_003235.5:c.8038A>G MANE Select	NP_003226.4:p.Thr2680Ala