Canonical Allele Identifier: CA372233814

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134030201G>C (hg19) ; chr8:g.133017956G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133017956G>C , CM000670.2:g.133017956G>C	GRCh38
NC_000008.10:g.134030201G>C , CM000670.1:g.134030201G>C	GRCh37
NC_000008.9:g.134099383G>C	NCBI36
NG_015832.1:g.155997G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.6741G>C MANE Select	ENSP00000220616.4:p.Glu2247Asp
ENST00000220616.8:c.6741G>C	ENSP00000220616.4:p.Glu2247Asp
ENST00000518108.1:c.168+90G>C
ENST00000519178.5:c.2107G>C
ENST00000519543.5:c.1140G>C	ENSP00000430430.1:p.Glu380Asp
ENST00000522523.5:n.802G>C
ENST00000523756.5:c.3396G>C
NM_003235.4:c.6741G>C	NP_003226.4:p.Glu2247Asp
XM_005251038.3:c.6549G>C	XP_005251095.1:p.Glu2183Asp
XM_006716622.2:c.6678G>C	XP_006716685.1:p.Glu2226Asp
XM_005251038.4:c.6549G>C	XP_005251095.1:p.Glu2183Asp
XM_006716622.3:c.6678G>C	XP_006716685.1:p.Glu2226Asp
XM_017013793.1:c.6675G>C	XP_016869282.1:p.Glu2225Asp
XM_017013794.1:c.6741G>C	XP_016869283.1:p.Glu2247Asp
XM_017013795.1:c.6570G>C	XP_016869284.1:p.Glu2190Asp
XM_017013796.1:c.6522G>C	XP_016869285.1:p.Glu2174Asp
XM_017013797.1:c.6480G>C	XP_016869286.1:p.Glu2160Asp
XM_017013798.1:c.6741G>C	XP_016869287.1:p.Glu2247Asp
NM_003235.5:c.6741G>C MANE Select	NP_003226.4:p.Glu2247Asp