Canonical Allele Identifier: CA372253448

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145834T>G (hg19) ; chr8:g.133133590T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133590T>G , CM000670.2:g.133133590T>G	GRCh38
NC_000008.10:g.134145834T>G , CM000670.1:g.134145834T>G	GRCh37
NC_000008.9:g.134215016T>G	NCBI36
NG_015832.1:g.271630T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8118T>G MANE Select	ENSP00000220616.4:p.Asn2706Lys
ENST00000220616.8:c.8118T>G	ENSP00000220616.4:p.Asn2706Lys
ENST00000519178.5:c.3484T>G
ENST00000519543.5:c.2517T>G	ENSP00000430430.1:p.Asn839Lys
ENST00000521107.1:c.330T>G	ENSP00000430161.1:p.Asn110Lys
ENST00000522691.1:n.204T>G
ENST00000523756.5:c.4773T>G
NM_003235.4:c.8118T>G	NP_003226.4:p.Asn2706Lys
XM_005251038.3:c.7926T>G	XP_005251095.1:p.Asn2642Lys
XM_006716622.2:c.8055T>G	XP_006716685.1:p.Asn2685Lys
XM_005251038.4:c.7926T>G	XP_005251095.1:p.Asn2642Lys
XM_006716622.3:c.8055T>G	XP_006716685.1:p.Asn2685Lys
XM_017013793.1:c.8052T>G	XP_016869282.1:p.Asn2684Lys
XM_017013794.1:c.7983T>G	XP_016869283.1:p.Asn2661Lys
XM_017013795.1:c.7947T>G	XP_016869284.1:p.Asn2649Lys
XM_017013796.1:c.7899T>G	XP_016869285.1:p.Asn2633Lys
XM_017013797.1:c.7857T>G	XP_016869286.1:p.Asn2619Lys
NM_003235.5:c.8118T>G MANE Select	NP_003226.4:p.Asn2706Lys