Canonical Allele Identifier: CA372253081

Gene: TG

Linked Data

• gnomAD v4: 8-133133498-C-G
• MyVariant Identifiers: chr8:g.134145742C>G (hg19) ; chr8:g.133133498C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133498C>G , CM000670.2:g.133133498C>G	GRCh38
NC_000008.10:g.134145742C>G , CM000670.1:g.134145742C>G	GRCh37
NC_000008.9:g.134214924C>G	NCBI36
NG_015832.1:g.271538C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8026C>G MANE Select	ENSP00000220616.4:p.Arg2676Gly
ENST00000220616.8:c.8026C>G	ENSP00000220616.4:p.Arg2676Gly
ENST00000519178.5:c.3392C>G
ENST00000519543.5:c.2425C>G	ENSP00000430430.1:p.Arg809Gly
ENST00000521107.1:c.238C>G	ENSP00000430161.1:p.Arg80Gly
ENST00000522691.1:n.112C>G
ENST00000523756.5:c.4681C>G
NM_003235.4:c.8026C>G	NP_003226.4:p.Arg2676Gly
XM_005251038.3:c.7834C>G	XP_005251095.1:p.Arg2612Gly
XM_006716622.2:c.7963C>G	XP_006716685.1:p.Arg2655Gly
XM_005251038.4:c.7834C>G	XP_005251095.1:p.Arg2612Gly
XM_006716622.3:c.7963C>G	XP_006716685.1:p.Arg2655Gly
XM_017013793.1:c.7960C>G	XP_016869282.1:p.Arg2654Gly
XM_017013794.1:c.7891C>G	XP_016869283.1:p.Arg2631Gly
XM_017013795.1:c.7855C>G	XP_016869284.1:p.Arg2619Gly
XM_017013796.1:c.7807C>G	XP_016869285.1:p.Arg2603Gly
XM_017013797.1:c.7765C>G	XP_016869286.1:p.Arg2589Gly
NM_003235.5:c.8026C>G MANE Select	NP_003226.4:p.Arg2676Gly