Canonical Allele Identifier: CA372253451

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145835C>G (hg19) ; chr8:g.133133591C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133591C>G , CM000670.2:g.133133591C>G	GRCh38
NC_000008.10:g.134145835C>G , CM000670.1:g.134145835C>G	GRCh37
NC_000008.9:g.134215017C>G	NCBI36
NG_015832.1:g.271631C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8119C>G MANE Select	ENSP00000220616.4:p.Arg2707Gly
ENST00000220616.8:c.8119C>G	ENSP00000220616.4:p.Arg2707Gly
ENST00000519178.5:c.3485C>G
ENST00000519543.5:c.2518C>G	ENSP00000430430.1:p.Arg840Gly
ENST00000521107.1:c.331C>G	ENSP00000430161.1:p.Arg111Gly
ENST00000522691.1:n.205C>G
ENST00000523756.5:c.4774C>G
NM_003235.4:c.8119C>G	NP_003226.4:p.Arg2707Gly
XM_005251038.3:c.7927C>G	XP_005251095.1:p.Arg2643Gly
XM_006716622.2:c.8056C>G	XP_006716685.1:p.Arg2686Gly
XM_005251038.4:c.7927C>G	XP_005251095.1:p.Arg2643Gly
XM_006716622.3:c.8056C>G	XP_006716685.1:p.Arg2686Gly
XM_017013793.1:c.8053C>G	XP_016869282.1:p.Arg2685Gly
XM_017013794.1:c.7984C>G	XP_016869283.1:p.Arg2662Gly
XM_017013795.1:c.7948C>G	XP_016869284.1:p.Arg2650Gly
XM_017013796.1:c.7900C>G	XP_016869285.1:p.Arg2634Gly
XM_017013797.1:c.7858C>G	XP_016869286.1:p.Arg2620Gly
NM_003235.5:c.8119C>G MANE Select	NP_003226.4:p.Arg2707Gly