Canonical Allele Identifier: CA463017019

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145744G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133500G>C , CM000670.2:g.133133500G>C	GRCh38
NC_000008.10:g.134145744G>C , CM000670.1:g.134145744G>C	GRCh37
NC_000008.9:g.134214926G>C	NCBI36
NG_015832.1:g.271540G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8028G>C MANE Select	ENSP00000220616.4:p.Arg2676=
ENST00000220616.8:c.8028G>C	ENSP00000220616.4:p.Arg2676=
ENST00000519178.5:c.3394G>C
ENST00000519543.5:c.2427G>C	ENSP00000430430.1:p.Arg809=
ENST00000521107.1:c.240G>C	ENSP00000430161.1:p.Arg80=
ENST00000522691.1:n.114G>C
ENST00000523756.5:c.4683G>C
NM_003235.4:c.8028G>C	NP_003226.4:p.Arg2676=
XM_005251038.3:c.7836G>C	XP_005251095.1:p.Arg2612=
XM_006716622.2:c.7965G>C	XP_006716685.1:p.Arg2655=
XM_005251038.4:c.7836G>C	XP_005251095.1:p.Arg2612=
XM_006716622.3:c.7965G>C	XP_006716685.1:p.Arg2655=
XM_017013793.1:c.7962G>C	XP_016869282.1:p.Arg2654=
XM_017013794.1:c.7893G>C	XP_016869283.1:p.Arg2631=
XM_017013795.1:c.7857G>C	XP_016869284.1:p.Arg2619=
XM_017013796.1:c.7809G>C	XP_016869285.1:p.Arg2603=
XM_017013797.1:c.7767G>C	XP_016869286.1:p.Arg2589=
NM_003235.5:c.8028G>C MANE Select	NP_003226.4:p.Arg2676=