Canonical Allele Identifier: CA463017262

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145873C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133629C>A , CM000670.2:g.133133629C>A	GRCh38
NC_000008.10:g.134145873C>A , CM000670.1:g.134145873C>A	GRCh37
NC_000008.9:g.134215055C>A	NCBI36
NG_015832.1:g.271669C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8157C>A MANE Select	ENSP00000220616.4:p.Ser2719=
ENST00000220616.8:c.8157C>A	ENSP00000220616.4:p.Ser2719=
ENST00000519178.5:c.3523C>A
ENST00000519543.5:c.2556C>A	ENSP00000430430.1:p.Ser852=
ENST00000521107.1:c.369C>A	ENSP00000430161.1:p.Ser123=
ENST00000522691.1:n.243C>A
ENST00000523756.5:c.4812C>A
NM_003235.4:c.8157C>A	NP_003226.4:p.Ser2719=
XM_005251038.3:c.7965C>A	XP_005251095.1:p.Ser2655=
XM_006716622.2:c.8094C>A	XP_006716685.1:p.Ser2698=
XM_005251038.4:c.7965C>A	XP_005251095.1:p.Ser2655=
XM_006716622.3:c.8094C>A	XP_006716685.1:p.Ser2698=
XM_017013793.1:c.8091C>A	XP_016869282.1:p.Ser2697=
XM_017013794.1:c.8022C>A	XP_016869283.1:p.Ser2674=
XM_017013795.1:c.7986C>A	XP_016869284.1:p.Ser2662=
XM_017013796.1:c.7938C>A	XP_016869285.1:p.Ser2646=
XM_017013797.1:c.7896C>A	XP_016869286.1:p.Ser2632=
NM_003235.5:c.8157C>A MANE Select	NP_003226.4:p.Ser2719=