Canonical Allele Identifier: CA463009516

Gene: TG

Linked Data

• ClinVar Variation Id: 2829008
• ClinVar RCV Id: RCV003686156
• MyVariant Identifiers: chr8:g.133911066C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132898821C>A , CM000670.2:g.132898821C>A	GRCh38
NC_000008.10:g.133911066C>A , CM000670.1:g.133911066C>A	GRCh37
NC_000008.9:g.133980248C>A	NCBI36
NG_015832.1:g.36862C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.3241C>A MANE Select	ENSP00000220616.4:p.Arg1081=
ENST00000220616.8:c.3241C>A	ENSP00000220616.4:p.Arg1081=
ENST00000518097.1:n.155C>A
ENST00000518505.1:c.141C>A
ENST00000523756.5:c.200C>A
NM_003235.4:c.3241C>A	NP_003226.4:p.Arg1081=
XM_005251038.3:c.3241C>A	XP_005251095.1:p.Arg1081=
XM_005251040.3:c.3241C>A	XP_005251097.1:p.Arg1081=
XM_005251042.3:c.3241C>A	XP_005251099.1:p.Arg1081=
XM_005251043.3:c.3241C>A	XP_005251100.1:p.Arg1081=
XM_006716622.2:c.3241C>A	XP_006716685.1:p.Arg1081=
XM_005251038.4:c.3241C>A	XP_005251095.1:p.Arg1081=
XM_005251040.4:c.3241C>A	XP_005251097.1:p.Arg1081=
XM_005251042.4:c.3241C>A	XP_005251099.1:p.Arg1081=
XM_006716622.3:c.3241C>A	XP_006716685.1:p.Arg1081=
XM_017013793.1:c.3241C>A	XP_016869282.1:p.Arg1081=
XM_017013794.1:c.3241C>A	XP_016869283.1:p.Arg1081=
XM_017013795.1:c.3241C>A	XP_016869284.1:p.Arg1081=
XM_017013796.1:c.3241C>A	XP_016869285.1:p.Arg1081=
XM_017013797.1:c.2980C>A	XP_016869286.1:p.Arg994=
XM_017013798.1:c.3241C>A	XP_016869287.1:p.Arg1081=
XM_017013799.1:c.3241C>A	XP_016869288.1:p.Arg1081=
XM_017013800.1:c.3241C>A	XP_016869289.1:p.Arg1081=
NM_003235.5:c.3241C>A MANE Select	NP_003226.4:p.Arg1081=