Canonical Allele Identifier: CA372252960

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145714A>C (hg19) ; chr8:g.133133470A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133470A>C , CM000670.2:g.133133470A>C	GRCh38
NC_000008.10:g.134145714A>C , CM000670.1:g.134145714A>C	GRCh37
NC_000008.9:g.134214896A>C	NCBI36
NG_015832.1:g.271510A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.7998A>C MANE Select	ENSP00000220616.4:p.Gly2666=
ENST00000220616.8:c.7998A>C	ENSP00000220616.4:p.Gly2666=
ENST00000519178.5:c.3364A>C
ENST00000519543.5:c.2397A>C	ENSP00000430430.1:p.Gly799=
ENST00000521107.1:c.210A>C	ENSP00000430161.1:p.Arg70Ser
ENST00000522691.1:n.84A>C
ENST00000523756.5:c.4653A>C
NM_003235.4:c.7998A>C	NP_003226.4:p.Gly2666=
XM_005251038.3:c.7806A>C	XP_005251095.1:p.Gly2602=
XM_006716622.2:c.7935A>C	XP_006716685.1:p.Gly2645=
XM_005251038.4:c.7806A>C	XP_005251095.1:p.Gly2602=
XM_006716622.3:c.7935A>C	XP_006716685.1:p.Gly2645=
XM_017013793.1:c.7932A>C	XP_016869282.1:p.Gly2644=
XM_017013794.1:c.7863A>C	XP_016869283.1:p.Arg2621Ser
XM_017013795.1:c.7827A>C	XP_016869284.1:p.Gly2609=
XM_017013796.1:c.7779A>C	XP_016869285.1:p.Gly2593=
XM_017013797.1:c.7737A>C	XP_016869286.1:p.Gly2579=
NM_003235.5:c.7998A>C MANE Select	NP_003226.4:p.Gly2666=