Canonical Allele Identifier: CA372253680

Gene: TG

Linked Data

• gnomAD v4: 8-133133648-A-G
• MyVariant Identifiers: chr8:g.134145892A>G (hg19) ; chr8:g.133133648A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133648A>G , CM000670.2:g.133133648A>G	GRCh38
NC_000008.10:g.134145892A>G , CM000670.1:g.134145892A>G	GRCh37
NC_000008.9:g.134215074A>G	NCBI36
NG_015832.1:g.271688A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8176A>G MANE Select	ENSP00000220616.4:p.Lys2726Glu
ENST00000220616.8:c.8176A>G	ENSP00000220616.4:p.Lys2726Glu
ENST00000519178.5:c.3542A>G
ENST00000519543.5:c.2575A>G	ENSP00000430430.1:p.Lys859Glu
ENST00000521107.1:c.388A>G	ENSP00000430161.1:p.Lys130Glu
ENST00000522691.1:n.262A>G
ENST00000523756.5:c.4831A>G
NM_003235.4:c.8176A>G	NP_003226.4:p.Lys2726Glu
XM_005251038.3:c.7984A>G	XP_005251095.1:p.Lys2662Glu
XM_006716622.2:c.8113A>G	XP_006716685.1:p.Lys2705Glu
XM_005251038.4:c.7984A>G	XP_005251095.1:p.Lys2662Glu
XM_006716622.3:c.8113A>G	XP_006716685.1:p.Lys2705Glu
XM_017013793.1:c.8110A>G	XP_016869282.1:p.Lys2704Glu
XM_017013794.1:c.8041A>G	XP_016869283.1:p.Lys2681Glu
XM_017013795.1:c.8005A>G	XP_016869284.1:p.Lys2669Glu
XM_017013796.1:c.7957A>G	XP_016869285.1:p.Lys2653Glu
XM_017013797.1:c.7915A>G	XP_016869286.1:p.Lys2639Glu
NM_003235.5:c.8176A>G MANE Select	NP_003226.4:p.Lys2726Glu