Canonical Allele Identifier: CA372253086

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145743G>T (hg19) ; chr8:g.133133499G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133499G>T , CM000670.2:g.133133499G>T	GRCh38
NC_000008.10:g.134145743G>T , CM000670.1:g.134145743G>T	GRCh37
NC_000008.9:g.134214925G>T	NCBI36
NG_015832.1:g.271539G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8027G>T MANE Select	ENSP00000220616.4:p.Arg2676Leu
ENST00000220616.8:c.8027G>T	ENSP00000220616.4:p.Arg2676Leu
ENST00000519178.5:c.3393G>T
ENST00000519543.5:c.2426G>T	ENSP00000430430.1:p.Arg809Leu
ENST00000521107.1:c.239G>T	ENSP00000430161.1:p.Arg80Leu
ENST00000522691.1:n.113G>T
ENST00000523756.5:c.4682G>T
NM_003235.4:c.8027G>T	NP_003226.4:p.Arg2676Leu
XM_005251038.3:c.7835G>T	XP_005251095.1:p.Arg2612Leu
XM_006716622.2:c.7964G>T	XP_006716685.1:p.Arg2655Leu
XM_005251038.4:c.7835G>T	XP_005251095.1:p.Arg2612Leu
XM_006716622.3:c.7964G>T	XP_006716685.1:p.Arg2655Leu
XM_017013793.1:c.7961G>T	XP_016869282.1:p.Arg2654Leu
XM_017013794.1:c.7892G>T	XP_016869283.1:p.Arg2631Leu
XM_017013795.1:c.7856G>T	XP_016869284.1:p.Arg2619Leu
XM_017013796.1:c.7808G>T	XP_016869285.1:p.Arg2603Leu
XM_017013797.1:c.7766G>T	XP_016869286.1:p.Arg2589Leu
NM_003235.5:c.8027G>T MANE Select	NP_003226.4:p.Arg2676Leu