Canonical Allele Identifier: CA372253400

Gene: TG

Linked Data

• dbSNP Id: rs2130424295
• MyVariant Identifiers: chr8:g.134145821A>C (hg19) ; chr8:g.133133577A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133577A>C , CM000670.2:g.133133577A>C	GRCh38
NC_000008.10:g.134145821A>C , CM000670.1:g.134145821A>C	GRCh37
NC_000008.9:g.134215003A>C	NCBI36
NG_015832.1:g.271617A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8105A>C MANE Select	ENSP00000220616.4:p.Glu2702Ala
ENST00000220616.8:c.8105A>C	ENSP00000220616.4:p.Glu2702Ala
ENST00000519178.5:c.3471A>C
ENST00000519543.5:c.2504A>C	ENSP00000430430.1:p.Glu835Ala
ENST00000521107.1:c.317A>C	ENSP00000430161.1:p.Glu106Ala
ENST00000522691.1:n.191A>C
ENST00000523756.5:c.4760A>C
NM_003235.4:c.8105A>C	NP_003226.4:p.Glu2702Ala
XM_005251038.3:c.7913A>C	XP_005251095.1:p.Glu2638Ala
XM_006716622.2:c.8042A>C	XP_006716685.1:p.Glu2681Ala
XM_005251038.4:c.7913A>C	XP_005251095.1:p.Glu2638Ala
XM_006716622.3:c.8042A>C	XP_006716685.1:p.Glu2681Ala
XM_017013793.1:c.8039A>C	XP_016869282.1:p.Glu2680Ala
XM_017013794.1:c.7970A>C	XP_016869283.1:p.Glu2657Ala
XM_017013795.1:c.7934A>C	XP_016869284.1:p.Glu2645Ala
XM_017013796.1:c.7886A>C	XP_016869285.1:p.Glu2629Ala
XM_017013797.1:c.7844A>C	XP_016869286.1:p.Glu2615Ala
NM_003235.5:c.8105A>C MANE Select	NP_003226.4:p.Glu2702Ala