Canonical Allele Identifier: CA372252995

Gene: TG

Linked Data

• dbSNP Id: rs1852101448
• MyVariant Identifiers: chr8:g.134145721A>G (hg19) ; chr8:g.133133477A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133477A>G , CM000670.2:g.133133477A>G	GRCh38
NC_000008.10:g.134145721A>G , CM000670.1:g.134145721A>G	GRCh37
NC_000008.9:g.134214903A>G	NCBI36
NG_015832.1:g.271517A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8005A>G MANE Select	ENSP00000220616.4:p.Asn2669Asp
ENST00000220616.8:c.8005A>G	ENSP00000220616.4:p.Asn2669Asp
ENST00000519178.5:c.3371A>G
ENST00000519543.5:c.2404A>G	ENSP00000430430.1:p.Asn802Asp
ENST00000521107.1:c.217A>G	ENSP00000430161.1:p.Asn73Asp
ENST00000522691.1:n.91A>G
ENST00000523756.5:c.4660A>G
NM_003235.4:c.8005A>G	NP_003226.4:p.Asn2669Asp
XM_005251038.3:c.7813A>G	XP_005251095.1:p.Asn2605Asp
XM_006716622.2:c.7942A>G	XP_006716685.1:p.Asn2648Asp
XM_005251038.4:c.7813A>G	XP_005251095.1:p.Asn2605Asp
XM_006716622.3:c.7942A>G	XP_006716685.1:p.Asn2648Asp
XM_017013793.1:c.7939A>G	XP_016869282.1:p.Asn2647Asp
XM_017013794.1:c.7870A>G	XP_016869283.1:p.Asn2624Asp
XM_017013795.1:c.7834A>G	XP_016869284.1:p.Asn2612Asp
XM_017013796.1:c.7786A>G	XP_016869285.1:p.Asn2596Asp
XM_017013797.1:c.7744A>G	XP_016869286.1:p.Asn2582Asp
NM_003235.5:c.8005A>G MANE Select	NP_003226.4:p.Asn2669Asp