Canonical Allele Identifier: CA372234009

Gene: TG

Linked Data

• ClinVar Variation Id: 2300183
• ClinVar RCV Id: RCV002865893
• MyVariant Identifiers: chr8:g.133980054A>C (hg19) ; chr8:g.132967809A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.132967809A>C , CM000670.2:g.132967809A>C	GRCh38
NC_000008.10:g.133980054A>C , CM000670.1:g.133980054A>C	GRCh37
NC_000008.9:g.134049236A>C	NCBI36
NG_015832.1:g.105850A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000220616.9:c.5702A>C MANE Select	ENSP00000220616.4:p.His1901Pro
ENST00000220616.8:c.5702A>C	ENSP00000220616.4:p.His1901Pro
ENST00000518058.1:c.97A>C
ENST00000519178.5:c.1068A>C
ENST00000519543.5:c.164A>C	ENSP00000430430.1:p.His55Pro
ENST00000523756.5:c.2357A>C
NM_003235.4:c.5702A>C	NP_003226.4:p.His1901Pro
XM_005251038.3:c.5510A>C	XP_005251095.1:p.His1837Pro
XM_005251040.3:c.5702A>C	XP_005251097.1:p.His1901Pro
XM_005251042.3:c.5702A>C	XP_005251099.1:p.His1901Pro
XM_005251043.3:c.5702A>C	XP_005251100.1:p.His1901Pro
XM_006716622.2:c.5702A>C	XP_006716685.1:p.His1901Pro
XM_005251038.4:c.5510A>C	XP_005251095.1:p.His1837Pro
XM_005251040.4:c.5702A>C	XP_005251097.1:p.His1901Pro
XM_005251042.4:c.5702A>C	XP_005251099.1:p.His1901Pro
XM_006716622.3:c.5702A>C	XP_006716685.1:p.His1901Pro
XM_017013793.1:c.5636A>C	XP_016869282.1:p.His1879Pro
XM_017013794.1:c.5702A>C	XP_016869283.1:p.His1901Pro
XM_017013795.1:c.5531A>C	XP_016869284.1:p.His1844Pro
XM_017013796.1:c.5483A>C	XP_016869285.1:p.His1828Pro
XM_017013797.1:c.5441A>C	XP_016869286.1:p.His1814Pro
XM_017013798.1:c.5702A>C	XP_016869287.1:p.His1901Pro
XM_017013799.1:c.5702A>C	XP_016869288.1:p.His1901Pro
XM_017013800.1:c.5702A>C	XP_016869289.1:p.His1901Pro
NM_003235.5:c.5702A>C MANE Select	NP_003226.4:p.His1901Pro