Canonical Allele Identifier: CA372253478

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145842G>C (hg19) ; chr8:g.133133598G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133598G>C , CM000670.2:g.133133598G>C	GRCh38
NC_000008.10:g.134145842G>C , CM000670.1:g.134145842G>C	GRCh37
NC_000008.9:g.134215024G>C	NCBI36
NG_015832.1:g.271638G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8126G>C MANE Select	ENSP00000220616.4:p.Gly2709Ala
ENST00000220616.8:c.8126G>C	ENSP00000220616.4:p.Gly2709Ala
ENST00000519178.5:c.3492G>C
ENST00000519543.5:c.2525G>C	ENSP00000430430.1:p.Gly842Ala
ENST00000521107.1:c.338G>C	ENSP00000430161.1:p.Gly113Ala
ENST00000522691.1:n.212G>C
ENST00000523756.5:c.4781G>C
NM_003235.4:c.8126G>C	NP_003226.4:p.Gly2709Ala
XM_005251038.3:c.7934G>C	XP_005251095.1:p.Gly2645Ala
XM_006716622.2:c.8063G>C	XP_006716685.1:p.Gly2688Ala
XM_005251038.4:c.7934G>C	XP_005251095.1:p.Gly2645Ala
XM_006716622.3:c.8063G>C	XP_006716685.1:p.Gly2688Ala
XM_017013793.1:c.8060G>C	XP_016869282.1:p.Gly2687Ala
XM_017013794.1:c.7991G>C	XP_016869283.1:p.Gly2664Ala
XM_017013795.1:c.7955G>C	XP_016869284.1:p.Gly2652Ala
XM_017013796.1:c.7907G>C	XP_016869285.1:p.Gly2636Ala
XM_017013797.1:c.7865G>C	XP_016869286.1:p.Gly2622Ala
NM_003235.5:c.8126G>C MANE Select	NP_003226.4:p.Gly2709Ala