Canonical Allele Identifier: CA372253381

Gene: TG

Linked Data

• dbSNP Id: rs1852111269
• gnomAD v3: 8-133133572-C-A
• gnomAD v4: 8-133133572-C-A
• MyVariant Identifiers: chr8:g.134145816C>A (hg19) ; chr8:g.133133572C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133572C>A , CM000670.2:g.133133572C>A	GRCh38
NC_000008.10:g.134145816C>A , CM000670.1:g.134145816C>A	GRCh37
NC_000008.9:g.134214998C>A	NCBI36
NG_015832.1:g.271612C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8100C>A MANE Select	ENSP00000220616.4:p.Phe2700Leu
ENST00000220616.8:c.8100C>A	ENSP00000220616.4:p.Phe2700Leu
ENST00000519178.5:c.3466C>A
ENST00000519543.5:c.2499C>A	ENSP00000430430.1:p.Phe833Leu
ENST00000521107.1:c.312C>A	ENSP00000430161.1:p.Phe104Leu
ENST00000522691.1:n.186C>A
ENST00000523756.5:c.4755C>A
NM_003235.4:c.8100C>A	NP_003226.4:p.Phe2700Leu
XM_005251038.3:c.7908C>A	XP_005251095.1:p.Phe2636Leu
XM_006716622.2:c.8037C>A	XP_006716685.1:p.Phe2679Leu
XM_005251038.4:c.7908C>A	XP_005251095.1:p.Phe2636Leu
XM_006716622.3:c.8037C>A	XP_006716685.1:p.Phe2679Leu
XM_017013793.1:c.8034C>A	XP_016869282.1:p.Phe2678Leu
XM_017013794.1:c.7965C>A	XP_016869283.1:p.Phe2655Leu
XM_017013795.1:c.7929C>A	XP_016869284.1:p.Phe2643Leu
XM_017013796.1:c.7881C>A	XP_016869285.1:p.Phe2627Leu
XM_017013797.1:c.7839C>A	XP_016869286.1:p.Phe2613Leu
NM_003235.5:c.8100C>A MANE Select	NP_003226.4:p.Phe2700Leu