Canonical Allele Identifier: CA372236912

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.133984116A>G (hg19) ; chr8:g.132971871A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132971871A>G , CM000670.2:g.132971871A>G	GRCh38
NC_000008.10:g.133984116A>G , CM000670.1:g.133984116A>G	GRCh37
NC_000008.9:g.134053298A>G	NCBI36
NG_015832.1:g.109912A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6053A>G MANE Select	ENSP00000220616.4:p.Lys2018Arg
ENST00000220616.8:c.6053A>G	ENSP00000220616.4:p.Lys2018Arg
ENST00000519178.5:c.1419A>G
ENST00000519294.5:n.45A>G
ENST00000519543.5:c.515A>G	ENSP00000430430.1:p.Lys172Arg
ENST00000520089.5:n.162A>G
ENST00000520197.5:n.190A>G
ENST00000523756.5:c.2708A>G
ENST00000524151.5:n.21A>G
NM_003235.4:c.6053A>G	NP_003226.4:p.Lys2018Arg
XM_005251038.3:c.5861A>G	XP_005251095.1:p.Lys1954Arg
XM_005251040.3:c.6053A>G	XP_005251097.1:p.Lys2018Arg
XM_005251042.3:c.6053A>G	XP_005251099.1:p.Lys2018Arg
XM_005251043.3:c.6053A>G	XP_005251100.1:p.Lys2018Arg
XM_006716622.2:c.6053A>G	XP_006716685.1:p.Lys2018Arg
XM_005251038.4:c.5861A>G	XP_005251095.1:p.Lys1954Arg
XM_005251040.4:c.6053A>G	XP_005251097.1:p.Lys2018Arg
XM_005251042.4:c.6053A>G	XP_005251099.1:p.Lys2018Arg
XM_006716622.3:c.6053A>G	XP_006716685.1:p.Lys2018Arg
XM_017013793.1:c.5987A>G	XP_016869282.1:p.Lys1996Arg
XM_017013794.1:c.6053A>G	XP_016869283.1:p.Lys2018Arg
XM_017013795.1:c.5882A>G	XP_016869284.1:p.Lys1961Arg
XM_017013796.1:c.5834A>G	XP_016869285.1:p.Lys1945Arg
XM_017013797.1:c.5792A>G	XP_016869286.1:p.Lys1931Arg
XM_017013798.1:c.6053A>G	XP_016869287.1:p.Lys2018Arg
XM_017013799.1:c.6053A>G	XP_016869288.1:p.Lys2018Arg
XM_017013800.1:c.6053A>G	XP_016869289.1:p.Lys2018Arg
NM_003235.5:c.6053A>G MANE Select	NP_003226.4:p.Lys2018Arg