Canonical Allele Identifier: CA372253293

Gene: TG

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8081G>T MANE Select	ENSP00000220616.4:p.Gly2694Val
ENST00000220616.8:c.8081G>T	ENSP00000220616.4:p.Gly2694Val
ENST00000519178.5:c.3447G>T
ENST00000519543.5:c.2480G>T	ENSP00000430430.1:p.Gly827Val
ENST00000521107.1:c.293G>T	ENSP00000430161.1:p.Gly98Val
ENST00000522691.1:n.167G>T
ENST00000523756.5:c.4736G>T
NM_003235.4:c.8081G>T	NP_003226.4:p.Gly2694Val
XM_005251038.3:c.7889G>T	XP_005251095.1:p.Gly2630Val
XM_006716622.2:c.8018G>T	XP_006716685.1:p.Gly2673Val
XM_005251038.4:c.7889G>T	XP_005251095.1:p.Gly2630Val
XM_006716622.3:c.8018G>T	XP_006716685.1:p.Gly2673Val
XM_017013793.1:c.8015G>T	XP_016869282.1:p.Gly2672Val
XM_017013794.1:c.7946G>T	XP_016869283.1:p.Gly2649Val
XM_017013795.1:c.7910G>T	XP_016869284.1:p.Gly2637Val
XM_017013796.1:c.7862G>T	XP_016869285.1:p.Gly2621Val
XM_017013797.1:c.7820G>T	XP_016869286.1:p.Gly2607Val
NM_003235.5:c.8081G>T MANE Select	NP_003226.4:p.Gly2694Val