Canonical Allele Identifier: CA463012888

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.133984087C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132971842C>A , CM000670.2:g.132971842C>A	GRCh38
NC_000008.10:g.133984087C>A , CM000670.1:g.133984087C>A	GRCh37
NC_000008.9:g.134053269C>A	NCBI36
NG_015832.1:g.109883C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6024C>A MANE Select	ENSP00000220616.4:p.Gly2008=
ENST00000220616.8:c.6024C>A	ENSP00000220616.4:p.Gly2008=
ENST00000519178.5:c.1390C>A
ENST00000519294.5:n.16C>A
ENST00000519543.5:c.486C>A	ENSP00000430430.1:p.Gly162=
ENST00000520089.5:n.133C>A
ENST00000520197.5:n.161C>A
ENST00000523756.5:c.2679C>A
NM_003235.4:c.6024C>A	NP_003226.4:p.Gly2008=
XM_005251038.3:c.5832C>A	XP_005251095.1:p.Gly1944=
XM_005251040.3:c.6024C>A	XP_005251097.1:p.Gly2008=
XM_005251042.3:c.6024C>A	XP_005251099.1:p.Gly2008=
XM_005251043.3:c.6024C>A	XP_005251100.1:p.Gly2008=
XM_006716622.2:c.6024C>A	XP_006716685.1:p.Gly2008=
XM_005251038.4:c.5832C>A	XP_005251095.1:p.Gly1944=
XM_005251040.4:c.6024C>A	XP_005251097.1:p.Gly2008=
XM_005251042.4:c.6024C>A	XP_005251099.1:p.Gly2008=
XM_006716622.3:c.6024C>A	XP_006716685.1:p.Gly2008=
XM_017013793.1:c.5958C>A	XP_016869282.1:p.Gly1986=
XM_017013794.1:c.6024C>A	XP_016869283.1:p.Gly2008=
XM_017013795.1:c.5853C>A	XP_016869284.1:p.Gly1951=
XM_017013796.1:c.5805C>A	XP_016869285.1:p.Gly1935=
XM_017013797.1:c.5763C>A	XP_016869286.1:p.Gly1921=
XM_017013798.1:c.6024C>A	XP_016869287.1:p.Gly2008=
XM_017013799.1:c.6024C>A	XP_016869288.1:p.Gly2008=
XM_017013800.1:c.6024C>A	XP_016869289.1:p.Gly2008=
NM_003235.5:c.6024C>A MANE Select	NP_003226.4:p.Gly2008=