Canonical Allele Identifier: CA463013044

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134030201G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017956G>A , CM000670.2:g.133017956G>A	GRCh38
NC_000008.10:g.134030201G>A , CM000670.1:g.134030201G>A	GRCh37
NC_000008.9:g.134099383G>A	NCBI36
NG_015832.1:g.155997G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6741G>A MANE Select	ENSP00000220616.4:p.Glu2247=
ENST00000220616.8:c.6741G>A	ENSP00000220616.4:p.Glu2247=
ENST00000518108.1:c.168+90G>A
ENST00000519178.5:c.2107G>A
ENST00000519543.5:c.1140G>A	ENSP00000430430.1:p.Glu380=
ENST00000522523.5:n.802G>A
ENST00000523756.5:c.3396G>A
NM_003235.4:c.6741G>A	NP_003226.4:p.Glu2247=
XM_005251038.3:c.6549G>A	XP_005251095.1:p.Glu2183=
XM_006716622.2:c.6678G>A	XP_006716685.1:p.Glu2226=
XM_005251038.4:c.6549G>A	XP_005251095.1:p.Glu2183=
XM_006716622.3:c.6678G>A	XP_006716685.1:p.Glu2226=
XM_017013793.1:c.6675G>A	XP_016869282.1:p.Glu2225=
XM_017013794.1:c.6741G>A	XP_016869283.1:p.Glu2247=
XM_017013795.1:c.6570G>A	XP_016869284.1:p.Glu2190=
XM_017013796.1:c.6522G>A	XP_016869285.1:p.Glu2174=
XM_017013797.1:c.6480G>A	XP_016869286.1:p.Glu2160=
XM_017013798.1:c.6741G>A	XP_016869287.1:p.Glu2247=
NM_003235.5:c.6741G>A MANE Select	NP_003226.4:p.Glu2247=