Canonical Allele Identifier: CA372253538

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145858C>G (hg19) ; chr8:g.133133614C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133614C>G , CM000670.2:g.133133614C>G	GRCh38
NC_000008.10:g.134145858C>G , CM000670.1:g.134145858C>G	GRCh37
NC_000008.9:g.134215040C>G	NCBI36
NG_015832.1:g.271654C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8142C>G MANE Select	ENSP00000220616.4:p.Asp2714Glu
ENST00000220616.8:c.8142C>G	ENSP00000220616.4:p.Asp2714Glu
ENST00000519178.5:c.3508C>G
ENST00000519543.5:c.2541C>G	ENSP00000430430.1:p.Asp847Glu
ENST00000521107.1:c.354C>G	ENSP00000430161.1:p.Asp118Glu
ENST00000522691.1:n.228C>G
ENST00000523756.5:c.4797C>G
NM_003235.4:c.8142C>G	NP_003226.4:p.Asp2714Glu
XM_005251038.3:c.7950C>G	XP_005251095.1:p.Asp2650Glu
XM_006716622.2:c.8079C>G	XP_006716685.1:p.Asp2693Glu
XM_005251038.4:c.7950C>G	XP_005251095.1:p.Asp2650Glu
XM_006716622.3:c.8079C>G	XP_006716685.1:p.Asp2693Glu
XM_017013793.1:c.8076C>G	XP_016869282.1:p.Asp2692Glu
XM_017013794.1:c.8007C>G	XP_016869283.1:p.Asp2669Glu
XM_017013795.1:c.7971C>G	XP_016869284.1:p.Asp2657Glu
XM_017013796.1:c.7923C>G	XP_016869285.1:p.Asp2641Glu
XM_017013797.1:c.7881C>G	XP_016869286.1:p.Asp2627Glu
NM_003235.5:c.8142C>G MANE Select	NP_003226.4:p.Asp2714Glu