Canonical Allele Identifier: CA463017213

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145843C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133599C>A , CM000670.2:g.133133599C>A	GRCh38
NC_000008.10:g.134145843C>A , CM000670.1:g.134145843C>A	GRCh37
NC_000008.9:g.134215025C>A	NCBI36
NG_015832.1:g.271639C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8127C>A MANE Select	ENSP00000220616.4:p.Gly2709=
ENST00000220616.8:c.8127C>A	ENSP00000220616.4:p.Gly2709=
ENST00000519178.5:c.3493C>A
ENST00000519543.5:c.2526C>A	ENSP00000430430.1:p.Gly842=
ENST00000521107.1:c.339C>A	ENSP00000430161.1:p.Gly113=
ENST00000522691.1:n.213C>A
ENST00000523756.5:c.4782C>A
NM_003235.4:c.8127C>A	NP_003226.4:p.Gly2709=
XM_005251038.3:c.7935C>A	XP_005251095.1:p.Gly2645=
XM_006716622.2:c.8064C>A	XP_006716685.1:p.Gly2688=
XM_005251038.4:c.7935C>A	XP_005251095.1:p.Gly2645=
XM_006716622.3:c.8064C>A	XP_006716685.1:p.Gly2688=
XM_017013793.1:c.8061C>A	XP_016869282.1:p.Gly2687=
XM_017013794.1:c.7992C>A	XP_016869283.1:p.Gly2664=
XM_017013795.1:c.7956C>A	XP_016869284.1:p.Gly2652=
XM_017013796.1:c.7908C>A	XP_016869285.1:p.Gly2636=
XM_017013797.1:c.7866C>A	XP_016869286.1:p.Gly2622=
NM_003235.5:c.8127C>A MANE Select	NP_003226.4:p.Gly2709=