Canonical Allele Identifier: CA463013097

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134030231C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017986C>G , CM000670.2:g.133017986C>G	GRCh38
NC_000008.10:g.134030231C>G , CM000670.1:g.134030231C>G	GRCh37
NC_000008.9:g.134099413C>G	NCBI36
NG_015832.1:g.156027C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6771C>G MANE Select	ENSP00000220616.4:p.Ala2257=
ENST00000220616.8:c.6771C>G	ENSP00000220616.4:p.Ala2257=
ENST00000518108.1:c.168+120C>G
ENST00000519178.5:c.2137C>G
ENST00000519543.5:c.1170C>G	ENSP00000430430.1:p.Ala390=
ENST00000523756.5:c.3426C>G
NM_003235.4:c.6771C>G	NP_003226.4:p.Ala2257=
XM_005251038.3:c.6579C>G	XP_005251095.1:p.Ala2193=
XM_006716622.2:c.6708C>G	XP_006716685.1:p.Ala2236=
XM_005251038.4:c.6579C>G	XP_005251095.1:p.Ala2193=
XM_006716622.3:c.6708C>G	XP_006716685.1:p.Ala2236=
XM_017013793.1:c.6705C>G	XP_016869282.1:p.Ala2235=
XM_017013794.1:c.6771C>G	XP_016869283.1:p.Ala2257=
XM_017013795.1:c.6600C>G	XP_016869284.1:p.Ala2200=
XM_017013796.1:c.6552C>G	XP_016869285.1:p.Ala2184=
XM_017013797.1:c.6510C>G	XP_016869286.1:p.Ala2170=
XM_017013798.1:c.6771C>G	XP_016869287.1:p.Ala2257=
NM_003235.5:c.6771C>G MANE Select	NP_003226.4:p.Ala2257=