Canonical Allele Identifier: CA372253305

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145801G>T (hg19) ; chr8:g.133133557G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133557G>T , CM000670.2:g.133133557G>T	GRCh38
NC_000008.10:g.134145801G>T , CM000670.1:g.134145801G>T	GRCh37
NC_000008.9:g.134214983G>T	NCBI36
NG_015832.1:g.271597G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8085G>T MANE Select	ENSP00000220616.4:p.Glu2695Asp
ENST00000220616.8:c.8085G>T	ENSP00000220616.4:p.Glu2695Asp
ENST00000519178.5:c.3451G>T
ENST00000519543.5:c.2484G>T	ENSP00000430430.1:p.Glu828Asp
ENST00000521107.1:c.297G>T	ENSP00000430161.1:p.Glu99Asp
ENST00000522691.1:n.171G>T
ENST00000523756.5:c.4740G>T
NM_003235.4:c.8085G>T	NP_003226.4:p.Glu2695Asp
XM_005251038.3:c.7893G>T	XP_005251095.1:p.Glu2631Asp
XM_006716622.2:c.8022G>T	XP_006716685.1:p.Glu2674Asp
XM_005251038.4:c.7893G>T	XP_005251095.1:p.Glu2631Asp
XM_006716622.3:c.8022G>T	XP_006716685.1:p.Glu2674Asp
XM_017013793.1:c.8019G>T	XP_016869282.1:p.Glu2673Asp
XM_017013794.1:c.7950G>T	XP_016869283.1:p.Glu2650Asp
XM_017013795.1:c.7914G>T	XP_016869284.1:p.Glu2638Asp
XM_017013796.1:c.7866G>T	XP_016869285.1:p.Glu2622Asp
XM_017013797.1:c.7824G>T	XP_016869286.1:p.Glu2608Asp
NM_003235.5:c.8085G>T MANE Select	NP_003226.4:p.Glu2695Asp