Canonical Allele Identifier: CA372253563

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145863C>A (hg19) ; chr8:g.133133619C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133619C>A , CM000670.2:g.133133619C>A	GRCh38
NC_000008.10:g.134145863C>A , CM000670.1:g.134145863C>A	GRCh37
NC_000008.9:g.134215045C>A	NCBI36
NG_015832.1:g.271659C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8147C>A MANE Select	ENSP00000220616.4:p.Ser2716Tyr
ENST00000220616.8:c.8147C>A	ENSP00000220616.4:p.Ser2716Tyr
ENST00000519178.5:c.3513C>A
ENST00000519543.5:c.2546C>A	ENSP00000430430.1:p.Ser849Tyr
ENST00000521107.1:c.359C>A	ENSP00000430161.1:p.Ser120Tyr
ENST00000522691.1:n.233C>A
ENST00000523756.5:c.4802C>A
NM_003235.4:c.8147C>A	NP_003226.4:p.Ser2716Tyr
XM_005251038.3:c.7955C>A	XP_005251095.1:p.Ser2652Tyr
XM_006716622.2:c.8084C>A	XP_006716685.1:p.Ser2695Tyr
XM_005251038.4:c.7955C>A	XP_005251095.1:p.Ser2652Tyr
XM_006716622.3:c.8084C>A	XP_006716685.1:p.Ser2695Tyr
XM_017013793.1:c.8081C>A	XP_016869282.1:p.Ser2694Tyr
XM_017013794.1:c.8012C>A	XP_016869283.1:p.Ser2671Tyr
XM_017013795.1:c.7976C>A	XP_016869284.1:p.Ser2659Tyr
XM_017013796.1:c.7928C>A	XP_016869285.1:p.Ser2643Tyr
XM_017013797.1:c.7886C>A	XP_016869286.1:p.Ser2629Tyr
NM_003235.5:c.8147C>A MANE Select	NP_003226.4:p.Ser2716Tyr