Canonical Allele Identifier: CA372253164

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145763A>G (hg19) ; chr8:g.133133519A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133519A>G , CM000670.2:g.133133519A>G	GRCh38
NC_000008.10:g.134145763A>G , CM000670.1:g.134145763A>G	GRCh37
NC_000008.9:g.134214945A>G	NCBI36
NG_015832.1:g.271559A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8047A>G MANE Select	ENSP00000220616.4:p.Thr2683Ala
ENST00000220616.8:c.8047A>G	ENSP00000220616.4:p.Thr2683Ala
ENST00000519178.5:c.3413A>G
ENST00000519543.5:c.2446A>G	ENSP00000430430.1:p.Thr816Ala
ENST00000521107.1:c.259A>G	ENSP00000430161.1:p.Thr87Ala
ENST00000522691.1:n.133A>G
ENST00000523756.5:c.4702A>G
NM_003235.4:c.8047A>G	NP_003226.4:p.Thr2683Ala
XM_005251038.3:c.7855A>G	XP_005251095.1:p.Thr2619Ala
XM_006716622.2:c.7984A>G	XP_006716685.1:p.Thr2662Ala
XM_005251038.4:c.7855A>G	XP_005251095.1:p.Thr2619Ala
XM_006716622.3:c.7984A>G	XP_006716685.1:p.Thr2662Ala
XM_017013793.1:c.7981A>G	XP_016869282.1:p.Thr2661Ala
XM_017013794.1:c.7912A>G	XP_016869283.1:p.Thr2638Ala
XM_017013795.1:c.7876A>G	XP_016869284.1:p.Thr2626Ala
XM_017013796.1:c.7828A>G	XP_016869285.1:p.Thr2610Ala
XM_017013797.1:c.7786A>G	XP_016869286.1:p.Thr2596Ala
NM_003235.5:c.8047A>G MANE Select	NP_003226.4:p.Thr2683Ala