Canonical Allele Identifier: CA10630302

Gene: TG

Linked Data

• ClinVar Variation Id: 361944
• ClinVar RCV Id: RCV000272792
• dbSNP Id: rs745902921
• MyVariant Identifiers: chr8:g.133911066C>G (hg19) ; chr8:g.132898821C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.3241C>G MANE Select	ENSP00000220616.4:p.Arg1081Gly
ENST00000220616.8:c.3241C>G	ENSP00000220616.4:p.Arg1081Gly
ENST00000518097.1:n.155C>G
ENST00000518505.1:c.141C>G
ENST00000523756.5:c.200C>G
NM_003235.4:c.3241C>G	NP_003226.4:p.Arg1081Gly
XM_005251038.3:c.3241C>G	XP_005251095.1:p.Arg1081Gly
XM_005251040.3:c.3241C>G	XP_005251097.1:p.Arg1081Gly
XM_005251042.3:c.3241C>G	XP_005251099.1:p.Arg1081Gly
XM_005251043.3:c.3241C>G	XP_005251100.1:p.Arg1081Gly
XM_006716622.2:c.3241C>G	XP_006716685.1:p.Arg1081Gly
XM_005251038.4:c.3241C>G	XP_005251095.1:p.Arg1081Gly
XM_005251040.4:c.3241C>G	XP_005251097.1:p.Arg1081Gly
XM_005251042.4:c.3241C>G	XP_005251099.1:p.Arg1081Gly
XM_006716622.3:c.3241C>G	XP_006716685.1:p.Arg1081Gly
XM_017013793.1:c.3241C>G	XP_016869282.1:p.Arg1081Gly
XM_017013794.1:c.3241C>G	XP_016869283.1:p.Arg1081Gly
XM_017013795.1:c.3241C>G	XP_016869284.1:p.Arg1081Gly
XM_017013796.1:c.3241C>G	XP_016869285.1:p.Arg1081Gly
XM_017013797.1:c.2980C>G	XP_016869286.1:p.Arg994Gly
XM_017013798.1:c.3241C>G	XP_016869287.1:p.Arg1081Gly
XM_017013799.1:c.3241C>G	XP_016869288.1:p.Arg1081Gly
XM_017013800.1:c.3241C>G	XP_016869289.1:p.Arg1081Gly
NM_003235.5:c.3241C>G MANE Select	NP_003226.4:p.Arg1081Gly