Canonical Allele Identifier: CA372253358

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145811G>C (hg19) ; chr8:g.133133567G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133567G>C , CM000670.2:g.133133567G>C	GRCh38
NC_000008.10:g.134145811G>C , CM000670.1:g.134145811G>C	GRCh37
NC_000008.9:g.134214993G>C	NCBI36
NG_015832.1:g.271607G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8095G>C MANE Select	ENSP00000220616.4:p.Glu2699Gln
ENST00000220616.8:c.8095G>C	ENSP00000220616.4:p.Glu2699Gln
ENST00000519178.5:c.3461G>C
ENST00000519543.5:c.2494G>C	ENSP00000430430.1:p.Glu832Gln
ENST00000521107.1:c.307G>C	ENSP00000430161.1:p.Glu103Gln
ENST00000522691.1:n.181G>C
ENST00000523756.5:c.4750G>C
NM_003235.4:c.8095G>C	NP_003226.4:p.Glu2699Gln
XM_005251038.3:c.7903G>C	XP_005251095.1:p.Glu2635Gln
XM_006716622.2:c.8032G>C	XP_006716685.1:p.Glu2678Gln
XM_005251038.4:c.7903G>C	XP_005251095.1:p.Glu2635Gln
XM_006716622.3:c.8032G>C	XP_006716685.1:p.Glu2678Gln
XM_017013793.1:c.8029G>C	XP_016869282.1:p.Glu2677Gln
XM_017013794.1:c.7960G>C	XP_016869283.1:p.Glu2654Gln
XM_017013795.1:c.7924G>C	XP_016869284.1:p.Glu2642Gln
XM_017013796.1:c.7876G>C	XP_016869285.1:p.Glu2626Gln
XM_017013797.1:c.7834G>C	XP_016869286.1:p.Glu2612Gln
NM_003235.5:c.8095G>C MANE Select	NP_003226.4:p.Glu2699Gln