Canonical Allele Identifier: CA463017292

Gene: TG

Linked Data

• MyVariant Identifiers: chr8:g.134145891G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.133133647G>C , CM000670.2:g.133133647G>C	GRCh38
NC_000008.10:g.134145891G>C , CM000670.1:g.134145891G>C	GRCh37
NC_000008.9:g.134215073G>C	NCBI36
NG_015832.1:g.271687G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000220616.9:c.8175G>C MANE Select	ENSP00000220616.4:p.Leu2725=
ENST00000220616.8:c.8175G>C	ENSP00000220616.4:p.Leu2725=
ENST00000519178.5:c.3541G>C
ENST00000519543.5:c.2574G>C	ENSP00000430430.1:p.Leu858=
ENST00000521107.1:c.387G>C	ENSP00000430161.1:p.Leu129=
ENST00000522691.1:n.261G>C
ENST00000523756.5:c.4830G>C
NM_003235.4:c.8175G>C	NP_003226.4:p.Leu2725=
XM_005251038.3:c.7983G>C	XP_005251095.1:p.Leu2661=
XM_006716622.2:c.8112G>C	XP_006716685.1:p.Leu2704=
XM_005251038.4:c.7983G>C	XP_005251095.1:p.Leu2661=
XM_006716622.3:c.8112G>C	XP_006716685.1:p.Leu2704=
XM_017013793.1:c.8109G>C	XP_016869282.1:p.Leu2703=
XM_017013794.1:c.8040G>C	XP_016869283.1:p.Leu2680=
XM_017013795.1:c.8004G>C	XP_016869284.1:p.Leu2668=
XM_017013796.1:c.7956G>C	XP_016869285.1:p.Leu2652=
XM_017013797.1:c.7914G>C	XP_016869286.1:p.Leu2638=
NM_003235.5:c.8175G>C MANE Select	NP_003226.4:p.Leu2725=