Canonical Allele Identifier: CA372253471

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145841G>C (hg19) ; chr8:g.133133597G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133597G>C , CM000670.2:g.133133597G>C	GRCh38
NC_000008.10:g.134145841G>C , CM000670.1:g.134145841G>C	GRCh37
NC_000008.9:g.134215023G>C	NCBI36
NG_015832.1:g.271637G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8125G>C MANE Select	ENSP00000220616.4:p.Gly2709Arg
ENST00000220616.8:c.8125G>C	ENSP00000220616.4:p.Gly2709Arg
ENST00000519178.5:c.3491G>C
ENST00000519543.5:c.2524G>C	ENSP00000430430.1:p.Gly842Arg
ENST00000521107.1:c.337G>C	ENSP00000430161.1:p.Gly113Arg
ENST00000522691.1:n.211G>C
ENST00000523756.5:c.4780G>C
NM_003235.4:c.8125G>C	NP_003226.4:p.Gly2709Arg
XM_005251038.3:c.7933G>C	XP_005251095.1:p.Gly2645Arg
XM_006716622.2:c.8062G>C	XP_006716685.1:p.Gly2688Arg
XM_005251038.4:c.7933G>C	XP_005251095.1:p.Gly2645Arg
XM_006716622.3:c.8062G>C	XP_006716685.1:p.Gly2688Arg
XM_017013793.1:c.8059G>C	XP_016869282.1:p.Gly2687Arg
XM_017013794.1:c.7990G>C	XP_016869283.1:p.Gly2664Arg
XM_017013795.1:c.7954G>C	XP_016869284.1:p.Gly2652Arg
XM_017013796.1:c.7906G>C	XP_016869285.1:p.Gly2636Arg
XM_017013797.1:c.7864G>C	XP_016869286.1:p.Gly2622Arg
NM_003235.5:c.8125G>C MANE Select	NP_003226.4:p.Gly2709Arg