Canonical Allele Identifier: CA463017135

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145795T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133551T>C , CM000670.2:g.133133551T>C	GRCh38
NC_000008.10:g.134145795T>C , CM000670.1:g.134145795T>C	GRCh37
NC_000008.9:g.134214977T>C	NCBI36
NG_015832.1:g.271591T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8079T>C MANE Select	ENSP00000220616.4:p.Gly2693=
ENST00000220616.8:c.8079T>C	ENSP00000220616.4:p.Gly2693=
ENST00000519178.5:c.3445T>C
ENST00000519543.5:c.2478T>C	ENSP00000430430.1:p.Gly826=
ENST00000521107.1:c.291T>C	ENSP00000430161.1:p.Gly97=
ENST00000522691.1:n.165T>C
ENST00000523756.5:c.4734T>C
NM_003235.4:c.8079T>C	NP_003226.4:p.Gly2693=
XM_005251038.3:c.7887T>C	XP_005251095.1:p.Gly2629=
XM_006716622.2:c.8016T>C	XP_006716685.1:p.Gly2672=
XM_005251038.4:c.7887T>C	XP_005251095.1:p.Gly2629=
XM_006716622.3:c.8016T>C	XP_006716685.1:p.Gly2672=
XM_017013793.1:c.8013T>C	XP_016869282.1:p.Gly2671=
XM_017013794.1:c.7944T>C	XP_016869283.1:p.Gly2648=
XM_017013795.1:c.7908T>C	XP_016869284.1:p.Gly2636=
XM_017013796.1:c.7860T>C	XP_016869285.1:p.Gly2620=
XM_017013797.1:c.7818T>C	XP_016869286.1:p.Gly2606=
NM_003235.5:c.8079T>C MANE Select	NP_003226.4:p.Gly2693=