Canonical Allele Identifier: CA372253414

Gene: TG

Linked Data

• gnomAD v4: 8-133133580-T-G
• MyVariant Identifiers: chr8:g.134145824T>G (hg19) ; chr8:g.133133580T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133580T>G , CM000670.2:g.133133580T>G	GRCh38
NC_000008.10:g.134145824T>G , CM000670.1:g.134145824T>G	GRCh37
NC_000008.9:g.134215006T>G	NCBI36
NG_015832.1:g.271620T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8108T>G MANE Select	ENSP00000220616.4:p.Leu2703Arg
ENST00000220616.8:c.8108T>G	ENSP00000220616.4:p.Leu2703Arg
ENST00000519178.5:c.3474T>G
ENST00000519543.5:c.2507T>G	ENSP00000430430.1:p.Leu836Arg
ENST00000521107.1:c.320T>G	ENSP00000430161.1:p.Leu107Arg
ENST00000522691.1:n.194T>G
ENST00000523756.5:c.4763T>G
NM_003235.4:c.8108T>G	NP_003226.4:p.Leu2703Arg
XM_005251038.3:c.7916T>G	XP_005251095.1:p.Leu2639Arg
XM_006716622.2:c.8045T>G	XP_006716685.1:p.Leu2682Arg
XM_005251038.4:c.7916T>G	XP_005251095.1:p.Leu2639Arg
XM_006716622.3:c.8045T>G	XP_006716685.1:p.Leu2682Arg
XM_017013793.1:c.8042T>G	XP_016869282.1:p.Leu2681Arg
XM_017013794.1:c.7973T>G	XP_016869283.1:p.Leu2658Arg
XM_017013795.1:c.7937T>G	XP_016869284.1:p.Leu2646Arg
XM_017013796.1:c.7889T>G	XP_016869285.1:p.Leu2630Arg
XM_017013797.1:c.7847T>G	XP_016869286.1:p.Leu2616Arg
NM_003235.5:c.8108T>G MANE Select	NP_003226.4:p.Leu2703Arg