Canonical Allele Identifier: CA372253285

Gene: TG

Linked Data

• gnomAD v4: 8-133133552-G-C
• MyVariant Identifiers: chr8:g.134145796G>C (hg19) ; chr8:g.133133552G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133552G>C , CM000670.2:g.133133552G>C	GRCh38
NC_000008.10:g.134145796G>C , CM000670.1:g.134145796G>C	GRCh37
NC_000008.9:g.134214978G>C	NCBI36
NG_015832.1:g.271592G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8080G>C MANE Select	ENSP00000220616.4:p.Gly2694Arg
ENST00000220616.8:c.8080G>C	ENSP00000220616.4:p.Gly2694Arg
ENST00000519178.5:c.3446G>C
ENST00000519543.5:c.2479G>C	ENSP00000430430.1:p.Gly827Arg
ENST00000521107.1:c.292G>C	ENSP00000430161.1:p.Gly98Arg
ENST00000522691.1:n.166G>C
ENST00000523756.5:c.4735G>C
NM_003235.4:c.8080G>C	NP_003226.4:p.Gly2694Arg
XM_005251038.3:c.7888G>C	XP_005251095.1:p.Gly2630Arg
XM_006716622.2:c.8017G>C	XP_006716685.1:p.Gly2673Arg
XM_005251038.4:c.7888G>C	XP_005251095.1:p.Gly2630Arg
XM_006716622.3:c.8017G>C	XP_006716685.1:p.Gly2673Arg
XM_017013793.1:c.8014G>C	XP_016869282.1:p.Gly2672Arg
XM_017013794.1:c.7945G>C	XP_016869283.1:p.Gly2649Arg
XM_017013795.1:c.7909G>C	XP_016869284.1:p.Gly2637Arg
XM_017013796.1:c.7861G>C	XP_016869285.1:p.Gly2621Arg
XM_017013797.1:c.7819G>C	XP_016869286.1:p.Gly2607Arg
NM_003235.5:c.8080G>C MANE Select	NP_003226.4:p.Gly2694Arg