Canonical Allele Identifier: CA372253321

Gene: TG

Linked Data

• dbSNP Id: rs1852110180
• MyVariant Identifiers: chr8:g.134145805T>A (hg19) ; chr8:g.133133561T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8089T>A MANE Select	ENSP00000220616.4:p.Tyr2697Asn
ENST00000220616.8:c.8089T>A	ENSP00000220616.4:p.Tyr2697Asn
ENST00000519178.5:c.3455T>A
ENST00000519543.5:c.2488T>A	ENSP00000430430.1:p.Tyr830Asn
ENST00000521107.1:c.301T>A	ENSP00000430161.1:p.Tyr101Asn
ENST00000522691.1:n.175T>A
ENST00000523756.5:c.4744T>A
NM_003235.4:c.8089T>A	NP_003226.4:p.Tyr2697Asn
XM_005251038.3:c.7897T>A	XP_005251095.1:p.Tyr2633Asn
XM_006716622.2:c.8026T>A	XP_006716685.1:p.Tyr2676Asn
XM_005251038.4:c.7897T>A	XP_005251095.1:p.Tyr2633Asn
XM_006716622.3:c.8026T>A	XP_006716685.1:p.Tyr2676Asn
XM_017013793.1:c.8023T>A	XP_016869282.1:p.Tyr2675Asn
XM_017013794.1:c.7954T>A	XP_016869283.1:p.Tyr2652Asn
XM_017013795.1:c.7918T>A	XP_016869284.1:p.Tyr2640Asn
XM_017013796.1:c.7870T>A	XP_016869285.1:p.Tyr2624Asn
XM_017013797.1:c.7828T>A	XP_016869286.1:p.Tyr2610Asn
NM_003235.5:c.8089T>A MANE Select	NP_003226.4:p.Tyr2697Asn