Canonical Allele Identifier: CA372253375

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145815T>G (hg19) ; chr8:g.133133571T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133571T>G , CM000670.2:g.133133571T>G	GRCh38
NC_000008.10:g.134145815T>G , CM000670.1:g.134145815T>G	GRCh37
NC_000008.9:g.134214997T>G	NCBI36
NG_015832.1:g.271611T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8099T>G MANE Select	ENSP00000220616.4:p.Phe2700Cys
ENST00000220616.8:c.8099T>G	ENSP00000220616.4:p.Phe2700Cys
ENST00000519178.5:c.3465T>G
ENST00000519543.5:c.2498T>G	ENSP00000430430.1:p.Phe833Cys
ENST00000521107.1:c.311T>G	ENSP00000430161.1:p.Phe104Cys
ENST00000522691.1:n.185T>G
ENST00000523756.5:c.4754T>G
NM_003235.4:c.8099T>G	NP_003226.4:p.Phe2700Cys
XM_005251038.3:c.7907T>G	XP_005251095.1:p.Phe2636Cys
XM_006716622.2:c.8036T>G	XP_006716685.1:p.Phe2679Cys
XM_005251038.4:c.7907T>G	XP_005251095.1:p.Phe2636Cys
XM_006716622.3:c.8036T>G	XP_006716685.1:p.Phe2679Cys
XM_017013793.1:c.8033T>G	XP_016869282.1:p.Phe2678Cys
XM_017013794.1:c.7964T>G	XP_016869283.1:p.Phe2655Cys
XM_017013795.1:c.7928T>G	XP_016869284.1:p.Phe2643Cys
XM_017013796.1:c.7880T>G	XP_016869285.1:p.Phe2627Cys
XM_017013797.1:c.7838T>G	XP_016869286.1:p.Phe2613Cys
NM_003235.5:c.8099T>G MANE Select	NP_003226.4:p.Phe2700Cys