Canonical Allele Identifier: CA186356788

Gene: TG

Linked Data

• dbSNP Id: rs929650595
• MyVariant Identifiers: chr8:g.134145820G>A (hg19) ; chr8:g.133133576G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133576G>A , CM000670.2:g.133133576G>A	GRCh38
NC_000008.10:g.134145820G>A , CM000670.1:g.134145820G>A	GRCh37
NC_000008.9:g.134215002G>A	NCBI36
NG_015832.1:g.271616G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8104G>A MANE Select	ENSP00000220616.4:p.Glu2702Lys
ENST00000220616.8:c.8104G>A	ENSP00000220616.4:p.Glu2702Lys
ENST00000519178.5:c.3470G>A
ENST00000519543.5:c.2503G>A	ENSP00000430430.1:p.Glu835Lys
ENST00000521107.1:c.316G>A	ENSP00000430161.1:p.Glu106Lys
ENST00000522691.1:n.190G>A
ENST00000523756.5:c.4759G>A
NM_003235.4:c.8104G>A	NP_003226.4:p.Glu2702Lys
XM_005251038.3:c.7912G>A	XP_005251095.1:p.Glu2638Lys
XM_006716622.2:c.8041G>A	XP_006716685.1:p.Glu2681Lys
XM_005251038.4:c.7912G>A	XP_005251095.1:p.Glu2638Lys
XM_006716622.3:c.8041G>A	XP_006716685.1:p.Glu2681Lys
XM_017013793.1:c.8038G>A	XP_016869282.1:p.Glu2680Lys
XM_017013794.1:c.7969G>A	XP_016869283.1:p.Glu2657Lys
XM_017013795.1:c.7933G>A	XP_016869284.1:p.Glu2645Lys
XM_017013796.1:c.7885G>A	XP_016869285.1:p.Glu2629Lys
XM_017013797.1:c.7843G>A	XP_016869286.1:p.Glu2615Lys
NM_003235.5:c.8104G>A MANE Select	NP_003226.4:p.Glu2702Lys