Canonical Allele Identifier: CA2270404839

Gene: POLG2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.64496487T= , CM000679.2:g.64496487T=	GRCh38
NC_000017.10:g.62492605T= , CM000679.1:g.62492605T=	GRCh37
NC_000017.9:g.59923067T=	NCBI36
NG_013029.1:g.5580A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000539111.7:c.482A= MANE Select	ENSP00000442563.2:p.Glu161=
ENST00000585104.2:n.453A=
ENST00000671755.1:c.453A=
ENST00000673460.1:c.453A=
ENST00000539111.6:c.482A=	ENSP00000442563.2:p.Glu161=
ENST00000578997.1:c.224+45A=	ENSP00000464389.1:n.224+45A=
ENST00000585141.5:n.533A=
NM_007215.3:c.482A=	NP_009146.2:p.Glu161=
XM_006721651.2:c.482A=	XP_006721714.1:p.Glu161=
XR_243630.1:n.533A=
XR_934357.1:n.533A=
XR_934358.1:n.533A=
NM_007215.4:c.482A= MANE Select	NP_009146.2:p.Glu161=