Canonical Allele Identifier: CA372233875

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134030215C>G (hg19) ; chr8:g.133017970C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017970C>G , CM000670.2:g.133017970C>G	GRCh38
NC_000008.10:g.134030215C>G , CM000670.1:g.134030215C>G	GRCh37
NC_000008.9:g.134099397C>G	NCBI36
NG_015832.1:g.156011C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6755C>G MANE Select	ENSP00000220616.4:p.Thr2252Arg
ENST00000220616.8:c.6755C>G	ENSP00000220616.4:p.Thr2252Arg
ENST00000518108.1:c.168+104C>G
ENST00000519178.5:c.2121C>G
ENST00000519543.5:c.1154C>G	ENSP00000430430.1:p.Thr385Arg
ENST00000523756.5:c.3410C>G
NM_003235.4:c.6755C>G	NP_003226.4:p.Thr2252Arg
XM_005251038.3:c.6563C>G	XP_005251095.1:p.Thr2188Arg
XM_006716622.2:c.6692C>G	XP_006716685.1:p.Thr2231Arg
XM_005251038.4:c.6563C>G	XP_005251095.1:p.Thr2188Arg
XM_006716622.3:c.6692C>G	XP_006716685.1:p.Thr2231Arg
XM_017013793.1:c.6689C>G	XP_016869282.1:p.Thr2230Arg
XM_017013794.1:c.6755C>G	XP_016869283.1:p.Thr2252Arg
XM_017013795.1:c.6584C>G	XP_016869284.1:p.Thr2195Arg
XM_017013796.1:c.6536C>G	XP_016869285.1:p.Thr2179Arg
XM_017013797.1:c.6494C>G	XP_016869286.1:p.Thr2165Arg
XM_017013798.1:c.6755C>G	XP_016869287.1:p.Thr2252Arg
NM_003235.5:c.6755C>G MANE Select	NP_003226.4:p.Thr2252Arg