Canonical Allele Identifier: CA8713021
Gene: POLG2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000539111.7:c.466A>G MANE Select ENSP00000442563.2:p.Ile156Val
ENST00000585104.2:n.437A>G
ENST00000671755.1:c.437A>G
ENST00000673460.1:c.437A>G
ENST00000539111.6:c.466A>G ENSP00000442563.2:p.Ile156Val
ENST00000578997.1:c.224+29A>G ENSP00000464389.1:n.224+29A>G
ENST00000585141.5:n.517A>G
NM_007215.3:c.466A>G NP_009146.2:p.Ile156Val
XM_006721651.2:c.466A>G XP_006721714.1:p.Ile156Val
XR_243630.1:n.517A>G
XR_934357.1:n.517A>G
XR_934358.1:n.517A>G
NM_007215.4:c.466A>G MANE Select NP_009146.2:p.Ile156Val