Canonical Allele Identifier: CA4885911

Gene: TG

Linked Data

• dbSNP Id: rs752408881
• ExAC: 8:134145883 T / A
• gnomAD v2: 8-134145883-T-A
• gnomAD v4: 8-133133639-T-A
• MyVariant Identifiers: chr8:g.134145883T>A (hg19) ; chr8:g.133133639T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133639T>A , CM000670.2:g.133133639T>A	GRCh38
NC_000008.10:g.134145883T>A , CM000670.1:g.134145883T>A	GRCh37
NC_000008.9:g.134215065T>A	NCBI36
NG_015832.1:g.271679T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8167T>A MANE Select	ENSP00000220616.4:p.Ser2723Thr
ENST00000220616.8:c.8167T>A	ENSP00000220616.4:p.Ser2723Thr
ENST00000519178.5:c.3533T>A
ENST00000519543.5:c.2566T>A	ENSP00000430430.1:p.Ser856Thr
ENST00000521107.1:c.379T>A	ENSP00000430161.1:p.Ser127Thr
ENST00000522691.1:n.253T>A
ENST00000523756.5:c.4822T>A
NM_003235.4:c.8167T>A	NP_003226.4:p.Ser2723Thr
XM_005251038.3:c.7975T>A	XP_005251095.1:p.Ser2659Thr
XM_006716622.2:c.8104T>A	XP_006716685.1:p.Ser2702Thr
XM_005251038.4:c.7975T>A	XP_005251095.1:p.Ser2659Thr
XM_006716622.3:c.8104T>A	XP_006716685.1:p.Ser2702Thr
XM_017013793.1:c.8101T>A	XP_016869282.1:p.Ser2701Thr
XM_017013794.1:c.8032T>A	XP_016869283.1:p.Ser2678Thr
XM_017013795.1:c.7996T>A	XP_016869284.1:p.Ser2666Thr
XM_017013796.1:c.7948T>A	XP_016869285.1:p.Ser2650Thr
XM_017013797.1:c.7906T>A	XP_016869286.1:p.Ser2636Thr
NM_003235.5:c.8167T>A MANE Select	NP_003226.4:p.Ser2723Thr