Canonical Allele Identifier: CA372253193

Gene: TG

Linked Data

• gnomAD v4: 8-133133527-G-T
• MyVariant Identifiers: chr8:g.134145771G>T (hg19) ; chr8:g.133133527G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133527G>T , CM000670.2:g.133133527G>T	GRCh38
NC_000008.10:g.134145771G>T , CM000670.1:g.134145771G>T	GRCh37
NC_000008.9:g.134214953G>T	NCBI36
NG_015832.1:g.271567G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8055G>T MANE Select	ENSP00000220616.4:p.Trp2685Cys
ENST00000220616.8:c.8055G>T	ENSP00000220616.4:p.Trp2685Cys
ENST00000519178.5:c.3421G>T
ENST00000519543.5:c.2454G>T	ENSP00000430430.1:p.Trp818Cys
ENST00000521107.1:c.267G>T	ENSP00000430161.1:p.Trp89Cys
ENST00000522691.1:n.141G>T
ENST00000523756.5:c.4710G>T
NM_003235.4:c.8055G>T	NP_003226.4:p.Trp2685Cys
XM_005251038.3:c.7863G>T	XP_005251095.1:p.Trp2621Cys
XM_006716622.2:c.7992G>T	XP_006716685.1:p.Trp2664Cys
XM_005251038.4:c.7863G>T	XP_005251095.1:p.Trp2621Cys
XM_006716622.3:c.7992G>T	XP_006716685.1:p.Trp2664Cys
XM_017013793.1:c.7989G>T	XP_016869282.1:p.Trp2663Cys
XM_017013794.1:c.7920G>T	XP_016869283.1:p.Trp2640Cys
XM_017013795.1:c.7884G>T	XP_016869284.1:p.Trp2628Cys
XM_017013796.1:c.7836G>T	XP_016869285.1:p.Trp2612Cys
XM_017013797.1:c.7794G>T	XP_016869286.1:p.Trp2598Cys
NM_003235.5:c.8055G>T MANE Select	NP_003226.4:p.Trp2685Cys