Canonical Allele Identifier: CA2270404845
Gene: POLG2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.64496503T= , CM000679.2:g.64496503T= GRCh38
NC_000017.10:g.62492621T= , CM000679.1:g.62492621T= GRCh37
NC_000017.9:g.59923083T= NCBI36
NG_013029.1:g.5564A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000539111.7:c.466A= MANE Select ENSP00000442563.2:p.Ile156=
ENST00000585104.2:n.437A=
ENST00000671755.1:c.437A=
ENST00000673460.1:c.437A=
ENST00000539111.6:c.466A= ENSP00000442563.2:p.Ile156=
ENST00000578997.1:c.224+29A= ENSP00000464389.1:n.224+29A=
ENST00000585141.5:n.517A=
NM_007215.3:c.466A= NP_009146.2:p.Ile156=
XM_006721651.2:c.466A= XP_006721714.1:p.Ile156=
XR_243630.1:n.517A=
XR_934357.1:n.517A=
XR_934358.1:n.517A=
NM_007215.4:c.466A= MANE Select NP_009146.2:p.Ile156=