Canonical Allele Identifier: CA463017067

Gene: TG

Linked Data

• gnomAD v4: 8-133133521-C-A
• MyVariant Identifiers: chr8:g.134145765C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133521C>A , CM000670.2:g.133133521C>A	GRCh38
NC_000008.10:g.134145765C>A , CM000670.1:g.134145765C>A	GRCh37
NC_000008.9:g.134214947C>A	NCBI36
NG_015832.1:g.271561C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8049C>A MANE Select	ENSP00000220616.4:p.Thr2683=
ENST00000220616.8:c.8049C>A	ENSP00000220616.4:p.Thr2683=
ENST00000519178.5:c.3415C>A
ENST00000519543.5:c.2448C>A	ENSP00000430430.1:p.Thr816=
ENST00000521107.1:c.261C>A	ENSP00000430161.1:p.Thr87=
ENST00000522691.1:n.135C>A
ENST00000523756.5:c.4704C>A
NM_003235.4:c.8049C>A	NP_003226.4:p.Thr2683=
XM_005251038.3:c.7857C>A	XP_005251095.1:p.Thr2619=
XM_006716622.2:c.7986C>A	XP_006716685.1:p.Thr2662=
XM_005251038.4:c.7857C>A	XP_005251095.1:p.Thr2619=
XM_006716622.3:c.7986C>A	XP_006716685.1:p.Thr2662=
XM_017013793.1:c.7983C>A	XP_016869282.1:p.Thr2661=
XM_017013794.1:c.7914C>A	XP_016869283.1:p.Thr2638=
XM_017013795.1:c.7878C>A	XP_016869284.1:p.Thr2626=
XM_017013796.1:c.7830C>A	XP_016869285.1:p.Thr2610=
XM_017013797.1:c.7788C>A	XP_016869286.1:p.Thr2596=
NM_003235.5:c.8049C>A MANE Select	NP_003226.4:p.Thr2683=