Canonical Allele Identifier: CA372253289

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145797G>A (hg19) ; chr8:g.133133553G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133553G>A , CM000670.2:g.133133553G>A	GRCh38
NC_000008.10:g.134145797G>A , CM000670.1:g.134145797G>A	GRCh37
NC_000008.9:g.134214979G>A	NCBI36
NG_015832.1:g.271593G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8081G>A MANE Select	ENSP00000220616.4:p.Gly2694Glu
ENST00000220616.8:c.8081G>A	ENSP00000220616.4:p.Gly2694Glu
ENST00000519178.5:c.3447G>A
ENST00000519543.5:c.2480G>A	ENSP00000430430.1:p.Gly827Glu
ENST00000521107.1:c.293G>A	ENSP00000430161.1:p.Gly98Glu
ENST00000522691.1:n.167G>A
ENST00000523756.5:c.4736G>A
NM_003235.4:c.8081G>A	NP_003226.4:p.Gly2694Glu
XM_005251038.3:c.7889G>A	XP_005251095.1:p.Gly2630Glu
XM_006716622.2:c.8018G>A	XP_006716685.1:p.Gly2673Glu
XM_005251038.4:c.7889G>A	XP_005251095.1:p.Gly2630Glu
XM_006716622.3:c.8018G>A	XP_006716685.1:p.Gly2673Glu
XM_017013793.1:c.8015G>A	XP_016869282.1:p.Gly2672Glu
XM_017013794.1:c.7946G>A	XP_016869283.1:p.Gly2649Glu
XM_017013795.1:c.7910G>A	XP_016869284.1:p.Gly2637Glu
XM_017013796.1:c.7862G>A	XP_016869285.1:p.Gly2621Glu
XM_017013797.1:c.7820G>A	XP_016869286.1:p.Gly2607Glu
NM_003235.5:c.8081G>A MANE Select	NP_003226.4:p.Gly2694Glu