Canonical Allele Identifier: CA463017206

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145837A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133593A>C , CM000670.2:g.133133593A>C	GRCh38
NC_000008.10:g.134145837A>C , CM000670.1:g.134145837A>C	GRCh37
NC_000008.9:g.134215019A>C	NCBI36
NG_015832.1:g.271633A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8121A>C MANE Select	ENSP00000220616.4:p.Arg2707=
ENST00000220616.8:c.8121A>C	ENSP00000220616.4:p.Arg2707=
ENST00000519178.5:c.3487A>C
ENST00000519543.5:c.2520A>C	ENSP00000430430.1:p.Arg840=
ENST00000521107.1:c.333A>C	ENSP00000430161.1:p.Arg111=
ENST00000522691.1:n.207A>C
ENST00000523756.5:c.4776A>C
NM_003235.4:c.8121A>C	NP_003226.4:p.Arg2707=
XM_005251038.3:c.7929A>C	XP_005251095.1:p.Arg2643=
XM_006716622.2:c.8058A>C	XP_006716685.1:p.Arg2686=
XM_005251038.4:c.7929A>C	XP_005251095.1:p.Arg2643=
XM_006716622.3:c.8058A>C	XP_006716685.1:p.Arg2686=
XM_017013793.1:c.8055A>C	XP_016869282.1:p.Arg2685=
XM_017013794.1:c.7986A>C	XP_016869283.1:p.Arg2662=
XM_017013795.1:c.7950A>C	XP_016869284.1:p.Arg2650=
XM_017013796.1:c.7902A>C	XP_016869285.1:p.Arg2634=
XM_017013797.1:c.7860A>C	XP_016869286.1:p.Arg2620=
NM_003235.5:c.8121A>C MANE Select	NP_003226.4:p.Arg2707=