Canonical Allele Identifier: CA372234011

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.133980055C>A (hg19) ; chr8:g.132967810C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132967810C>A , CM000670.2:g.132967810C>A	GRCh38
NC_000008.10:g.133980055C>A , CM000670.1:g.133980055C>A	GRCh37
NC_000008.9:g.134049237C>A	NCBI36
NG_015832.1:g.105851C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.5703C>A MANE Select	ENSP00000220616.4:p.His1901Gln
ENST00000220616.8:c.5703C>A	ENSP00000220616.4:p.His1901Gln
ENST00000518058.1:c.98C>A
ENST00000519178.5:c.1069C>A
ENST00000519543.5:c.165C>A	ENSP00000430430.1:p.His55Gln
ENST00000523756.5:c.2358C>A
NM_003235.4:c.5703C>A	NP_003226.4:p.His1901Gln
XM_005251038.3:c.5511C>A	XP_005251095.1:p.His1837Gln
XM_005251040.3:c.5703C>A	XP_005251097.1:p.His1901Gln
XM_005251042.3:c.5703C>A	XP_005251099.1:p.His1901Gln
XM_005251043.3:c.5703C>A	XP_005251100.1:p.His1901Gln
XM_006716622.2:c.5703C>A	XP_006716685.1:p.His1901Gln
XM_005251038.4:c.5511C>A	XP_005251095.1:p.His1837Gln
XM_005251040.4:c.5703C>A	XP_005251097.1:p.His1901Gln
XM_005251042.4:c.5703C>A	XP_005251099.1:p.His1901Gln
XM_006716622.3:c.5703C>A	XP_006716685.1:p.His1901Gln
XM_017013793.1:c.5637C>A	XP_016869282.1:p.His1879Gln
XM_017013794.1:c.5703C>A	XP_016869283.1:p.His1901Gln
XM_017013795.1:c.5532C>A	XP_016869284.1:p.His1844Gln
XM_017013796.1:c.5484C>A	XP_016869285.1:p.His1828Gln
XM_017013797.1:c.5442C>A	XP_016869286.1:p.His1814Gln
XM_017013798.1:c.5703C>A	XP_016869287.1:p.His1901Gln
XM_017013799.1:c.5703C>A	XP_016869288.1:p.His1901Gln
XM_017013800.1:c.5703C>A	XP_016869289.1:p.His1901Gln
NM_003235.5:c.5703C>A MANE Select	NP_003226.4:p.His1901Gln