Canonical Allele Identifier: CA372253328

Gene: TG

Linked Data

• dbSNP Id: rs1852110357
• MyVariant Identifiers: chr8:g.134145806A>G (hg19) ; chr8:g.133133562A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133562A>G , CM000670.2:g.133133562A>G	GRCh38
NC_000008.10:g.134145806A>G , CM000670.1:g.134145806A>G	GRCh37
NC_000008.9:g.134214988A>G	NCBI36
NG_015832.1:g.271602A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8090A>G MANE Select	ENSP00000220616.4:p.Tyr2697Cys
ENST00000220616.8:c.8090A>G	ENSP00000220616.4:p.Tyr2697Cys
ENST00000519178.5:c.3456A>G
ENST00000519543.5:c.2489A>G	ENSP00000430430.1:p.Tyr830Cys
ENST00000521107.1:c.302A>G	ENSP00000430161.1:p.Tyr101Cys
ENST00000522691.1:n.176A>G
ENST00000523756.5:c.4745A>G
NM_003235.4:c.8090A>G	NP_003226.4:p.Tyr2697Cys
XM_005251038.3:c.7898A>G	XP_005251095.1:p.Tyr2633Cys
XM_006716622.2:c.8027A>G	XP_006716685.1:p.Tyr2676Cys
XM_005251038.4:c.7898A>G	XP_005251095.1:p.Tyr2633Cys
XM_006716622.3:c.8027A>G	XP_006716685.1:p.Tyr2676Cys
XM_017013793.1:c.8024A>G	XP_016869282.1:p.Tyr2675Cys
XM_017013794.1:c.7955A>G	XP_016869283.1:p.Tyr2652Cys
XM_017013795.1:c.7919A>G	XP_016869284.1:p.Tyr2640Cys
XM_017013796.1:c.7871A>G	XP_016869285.1:p.Tyr2624Cys
XM_017013797.1:c.7829A>G	XP_016869286.1:p.Tyr2610Cys
NM_003235.5:c.8090A>G MANE Select	NP_003226.4:p.Tyr2697Cys