Canonical Allele Identifier: CA372253324

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145805T>G (hg19) ; chr8:g.133133561T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133561T>G , CM000670.2:g.133133561T>G	GRCh38
NC_000008.10:g.134145805T>G , CM000670.1:g.134145805T>G	GRCh37
NC_000008.9:g.134214987T>G	NCBI36
NG_015832.1:g.271601T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8089T>G MANE Select	ENSP00000220616.4:p.Tyr2697Asp
ENST00000220616.8:c.8089T>G	ENSP00000220616.4:p.Tyr2697Asp
ENST00000519178.5:c.3455T>G
ENST00000519543.5:c.2488T>G	ENSP00000430430.1:p.Tyr830Asp
ENST00000521107.1:c.301T>G	ENSP00000430161.1:p.Tyr101Asp
ENST00000522691.1:n.175T>G
ENST00000523756.5:c.4744T>G
NM_003235.4:c.8089T>G	NP_003226.4:p.Tyr2697Asp
XM_005251038.3:c.7897T>G	XP_005251095.1:p.Tyr2633Asp
XM_006716622.2:c.8026T>G	XP_006716685.1:p.Tyr2676Asp
XM_005251038.4:c.7897T>G	XP_005251095.1:p.Tyr2633Asp
XM_006716622.3:c.8026T>G	XP_006716685.1:p.Tyr2676Asp
XM_017013793.1:c.8023T>G	XP_016869282.1:p.Tyr2675Asp
XM_017013794.1:c.7954T>G	XP_016869283.1:p.Tyr2652Asp
XM_017013795.1:c.7918T>G	XP_016869284.1:p.Tyr2640Asp
XM_017013796.1:c.7870T>G	XP_016869285.1:p.Tyr2624Asp
XM_017013797.1:c.7828T>G	XP_016869286.1:p.Tyr2610Asp
NM_003235.5:c.8089T>G MANE Select	NP_003226.4:p.Tyr2697Asp