Canonical Allele Identifier: CA372253562

Gene: TG

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8147C>G MANE Select	ENSP00000220616.4:p.Ser2716Cys
ENST00000220616.8:c.8147C>G	ENSP00000220616.4:p.Ser2716Cys
ENST00000519178.5:c.3513C>G
ENST00000519543.5:c.2546C>G	ENSP00000430430.1:p.Ser849Cys
ENST00000521107.1:c.359C>G	ENSP00000430161.1:p.Ser120Cys
ENST00000522691.1:n.233C>G
ENST00000523756.5:c.4802C>G
NM_003235.4:c.8147C>G	NP_003226.4:p.Ser2716Cys
XM_005251038.3:c.7955C>G	XP_005251095.1:p.Ser2652Cys
XM_006716622.2:c.8084C>G	XP_006716685.1:p.Ser2695Cys
XM_005251038.4:c.7955C>G	XP_005251095.1:p.Ser2652Cys
XM_006716622.3:c.8084C>G	XP_006716685.1:p.Ser2695Cys
XM_017013793.1:c.8081C>G	XP_016869282.1:p.Ser2694Cys
XM_017013794.1:c.8012C>G	XP_016869283.1:p.Ser2671Cys
XM_017013795.1:c.7976C>G	XP_016869284.1:p.Ser2659Cys
XM_017013796.1:c.7928C>G	XP_016869285.1:p.Ser2643Cys
XM_017013797.1:c.7886C>G	XP_016869286.1:p.Ser2629Cys
NM_003235.5:c.8147C>G MANE Select	NP_003226.4:p.Ser2716Cys