Canonical Allele Identifier: CA463017097

Gene: TG

Linked Data

• dbSNP Id: rs1427199757
• MyVariant Identifiers: chr8:g.134145780T>C (hg19) ; chr8:g.133133536T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133536T>C , CM000670.2:g.133133536T>C	GRCh38
NC_000008.10:g.134145780T>C , CM000670.1:g.134145780T>C	GRCh37
NC_000008.9:g.134214962T>C	NCBI36
NG_015832.1:g.271576T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8064T>C MANE Select	ENSP00000220616.4:p.Phe2688=
ENST00000220616.8:c.8064T>C	ENSP00000220616.4:p.Phe2688=
ENST00000519178.5:c.3430T>C
ENST00000519543.5:c.2463T>C	ENSP00000430430.1:p.Phe821=
ENST00000521107.1:c.276T>C	ENSP00000430161.1:p.Phe92=
ENST00000522691.1:n.150T>C
ENST00000523756.5:c.4719T>C
NM_003235.4:c.8064T>C	NP_003226.4:p.Phe2688=
XM_005251038.3:c.7872T>C	XP_005251095.1:p.Phe2624=
XM_006716622.2:c.8001T>C	XP_006716685.1:p.Phe2667=
XM_005251038.4:c.7872T>C	XP_005251095.1:p.Phe2624=
XM_006716622.3:c.8001T>C	XP_006716685.1:p.Phe2667=
XM_017013793.1:c.7998T>C	XP_016869282.1:p.Phe2666=
XM_017013794.1:c.7929T>C	XP_016869283.1:p.Phe2643=
XM_017013795.1:c.7893T>C	XP_016869284.1:p.Phe2631=
XM_017013796.1:c.7845T>C	XP_016869285.1:p.Phe2615=
XM_017013797.1:c.7803T>C	XP_016869286.1:p.Phe2601=
NM_003235.5:c.8064T>C MANE Select	NP_003226.4:p.Phe2688=