Canonical Allele Identifier: CA372253473

Gene: TG

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8125G>A MANE Select	ENSP00000220616.4:p.Gly2709Ser
ENST00000220616.8:c.8125G>A	ENSP00000220616.4:p.Gly2709Ser
ENST00000519178.5:c.3491G>A
ENST00000519543.5:c.2524G>A	ENSP00000430430.1:p.Gly842Ser
ENST00000521107.1:c.337G>A	ENSP00000430161.1:p.Gly113Ser
ENST00000522691.1:n.211G>A
ENST00000523756.5:c.4780G>A
NM_003235.4:c.8125G>A	NP_003226.4:p.Gly2709Ser
XM_005251038.3:c.7933G>A	XP_005251095.1:p.Gly2645Ser
XM_006716622.2:c.8062G>A	XP_006716685.1:p.Gly2688Ser
XM_005251038.4:c.7933G>A	XP_005251095.1:p.Gly2645Ser
XM_006716622.3:c.8062G>A	XP_006716685.1:p.Gly2688Ser
XM_017013793.1:c.8059G>A	XP_016869282.1:p.Gly2687Ser
XM_017013794.1:c.7990G>A	XP_016869283.1:p.Gly2664Ser
XM_017013795.1:c.7954G>A	XP_016869284.1:p.Gly2652Ser
XM_017013796.1:c.7906G>A	XP_016869285.1:p.Gly2636Ser
XM_017013797.1:c.7864G>A	XP_016869286.1:p.Gly2622Ser
NM_003235.5:c.8125G>A MANE Select	NP_003226.4:p.Gly2709Ser