Canonical Allele Identifier: CA463017245

Gene: TG

Linked Data

• gnomAD v4: 8-133133617-C-T
• MyVariant Identifiers: chr8:g.134145861C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133617C>T , CM000670.2:g.133133617C>T	GRCh38
NC_000008.10:g.134145861C>T , CM000670.1:g.134145861C>T	GRCh37
NC_000008.9:g.134215043C>T	NCBI36
NG_015832.1:g.271657C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8145C>T MANE Select	ENSP00000220616.4:p.Cys2715=
ENST00000220616.8:c.8145C>T	ENSP00000220616.4:p.Cys2715=
ENST00000519178.5:c.3511C>T
ENST00000519543.5:c.2544C>T	ENSP00000430430.1:p.Cys848=
ENST00000521107.1:c.357C>T	ENSP00000430161.1:p.Cys119=
ENST00000522691.1:n.231C>T
ENST00000523756.5:c.4800C>T
NM_003235.4:c.8145C>T	NP_003226.4:p.Cys2715=
XM_005251038.3:c.7953C>T	XP_005251095.1:p.Cys2651=
XM_006716622.2:c.8082C>T	XP_006716685.1:p.Cys2694=
XM_005251038.4:c.7953C>T	XP_005251095.1:p.Cys2651=
XM_006716622.3:c.8082C>T	XP_006716685.1:p.Cys2694=
XM_017013793.1:c.8079C>T	XP_016869282.1:p.Cys2693=
XM_017013794.1:c.8010C>T	XP_016869283.1:p.Cys2670=
XM_017013795.1:c.7974C>T	XP_016869284.1:p.Cys2658=
XM_017013796.1:c.7926C>T	XP_016869285.1:p.Cys2642=
XM_017013797.1:c.7884C>T	XP_016869286.1:p.Cys2628=
NM_003235.5:c.8145C>T MANE Select	NP_003226.4:p.Cys2715=