Canonical Allele Identifier: CA372253683

Gene: TG

Linked Data

• dbSNP Id: rs1852117514
• gnomAD v4: 8-133133649-A-G
• MyVariant Identifiers: chr8:g.134145893A>G (hg19) ; chr8:g.133133649A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133649A>G , CM000670.2:g.133133649A>G	GRCh38
NC_000008.10:g.134145893A>G , CM000670.1:g.134145893A>G	GRCh37
NC_000008.9:g.134215075A>G	NCBI36
NG_015832.1:g.271689A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8177A>G MANE Select	ENSP00000220616.4:p.Lys2726Arg
ENST00000220616.8:c.8177A>G	ENSP00000220616.4:p.Lys2726Arg
ENST00000519178.5:c.3543A>G
ENST00000519543.5:c.2576A>G	ENSP00000430430.1:p.Lys859Arg
ENST00000521107.1:c.389A>G	ENSP00000430161.1:p.Lys130Arg
ENST00000522691.1:n.263A>G
ENST00000523756.5:c.4832A>G
NM_003235.4:c.8177A>G	NP_003226.4:p.Lys2726Arg
XM_005251038.3:c.7985A>G	XP_005251095.1:p.Lys2662Arg
XM_006716622.2:c.8114A>G	XP_006716685.1:p.Lys2705Arg
XM_005251038.4:c.7985A>G	XP_005251095.1:p.Lys2662Arg
XM_006716622.3:c.8114A>G	XP_006716685.1:p.Lys2705Arg
XM_017013793.1:c.8111A>G	XP_016869282.1:p.Lys2704Arg
XM_017013794.1:c.8042A>G	XP_016869283.1:p.Lys2681Arg
XM_017013795.1:c.8006A>G	XP_016869284.1:p.Lys2669Arg
XM_017013796.1:c.7958A>G	XP_016869285.1:p.Lys2653Arg
XM_017013797.1:c.7916A>G	XP_016869286.1:p.Lys2639Arg
NM_003235.5:c.8177A>G MANE Select	NP_003226.4:p.Lys2726Arg