Canonical Allele Identifier: CA463017166

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145816C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133572C>T , CM000670.2:g.133133572C>T	GRCh38
NC_000008.10:g.134145816C>T , CM000670.1:g.134145816C>T	GRCh37
NC_000008.9:g.134214998C>T	NCBI36
NG_015832.1:g.271612C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8100C>T MANE Select	ENSP00000220616.4:p.Phe2700=
ENST00000220616.8:c.8100C>T	ENSP00000220616.4:p.Phe2700=
ENST00000519178.5:c.3466C>T
ENST00000519543.5:c.2499C>T	ENSP00000430430.1:p.Phe833=
ENST00000521107.1:c.312C>T	ENSP00000430161.1:p.Phe104=
ENST00000522691.1:n.186C>T
ENST00000523756.5:c.4755C>T
NM_003235.4:c.8100C>T	NP_003226.4:p.Phe2700=
XM_005251038.3:c.7908C>T	XP_005251095.1:p.Phe2636=
XM_006716622.2:c.8037C>T	XP_006716685.1:p.Phe2679=
XM_005251038.4:c.7908C>T	XP_005251095.1:p.Phe2636=
XM_006716622.3:c.8037C>T	XP_006716685.1:p.Phe2679=
XM_017013793.1:c.8034C>T	XP_016869282.1:p.Phe2678=
XM_017013794.1:c.7965C>T	XP_016869283.1:p.Phe2655=
XM_017013795.1:c.7929C>T	XP_016869284.1:p.Phe2643=
XM_017013796.1:c.7881C>T	XP_016869285.1:p.Phe2627=
XM_017013797.1:c.7839C>T	XP_016869286.1:p.Phe2613=
NM_003235.5:c.8100C>T MANE Select	NP_003226.4:p.Phe2700=