Canonical Allele Identifier: CA463012100

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.133975291G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132963046G>A , CM000670.2:g.132963046G>A	GRCh38
NC_000008.10:g.133975291G>A , CM000670.1:g.133975291G>A	GRCh37
NC_000008.9:g.134044473G>A	NCBI36
NG_015832.1:g.101087G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.5520G>A MANE Select	ENSP00000220616.4:p.Val1840=
ENST00000220616.8:c.5520G>A	ENSP00000220616.4:p.Val1840=
ENST00000518058.1:c.53G>A
ENST00000519178.5:c.886G>A
ENST00000523756.5:c.2175G>A
NM_003235.4:c.5520G>A	NP_003226.4:p.Val1840=
XM_005251038.3:c.5328G>A	XP_005251095.1:p.Val1776=
XM_005251040.3:c.5520G>A	XP_005251097.1:p.Val1840=
XM_005251042.3:c.5520G>A	XP_005251099.1:p.Val1840=
XM_005251043.3:c.5520G>A	XP_005251100.1:p.Val1840=
XM_006716622.2:c.5520G>A	XP_006716685.1:p.Val1840=
XM_005251038.4:c.5328G>A	XP_005251095.1:p.Val1776=
XM_005251040.4:c.5520G>A	XP_005251097.1:p.Val1840=
XM_005251042.4:c.5520G>A	XP_005251099.1:p.Val1840=
XM_006716622.3:c.5520G>A	XP_006716685.1:p.Val1840=
XM_017013793.1:c.5454G>A	XP_016869282.1:p.Val1818=
XM_017013794.1:c.5520G>A	XP_016869283.1:p.Val1840=
XM_017013795.1:c.5349G>A	XP_016869284.1:p.Val1783=
XM_017013796.1:c.5301G>A	XP_016869285.1:p.Val1767=
XM_017013797.1:c.5259G>A	XP_016869286.1:p.Val1753=
XM_017013798.1:c.5520G>A	XP_016869287.1:p.Val1840=
XM_017013799.1:c.5520G>A	XP_016869288.1:p.Val1840=
XM_017013800.1:c.5520G>A	XP_016869289.1:p.Val1840=
NM_003235.5:c.5520G>A MANE Select	NP_003226.4:p.Val1840=