Canonical Allele Identifier: CA7725052
Gene: POLG HGNC NCBI

Linked Data

ClinVar Variation Id: 861889
dbSNP Id: rs367959489

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89330206G>C , CM000677.2:g.89330206G>C GRCh38
NC_000015.9:g.89873437G>C , CM000677.1:g.89873437G>C GRCh37
NC_000015.8:g.87674441G>C NCBI36
NG_008218.1:g.9590C>G
NG_008218.2:g.9590C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.730C>G ENSP00000516154.1:p.Leu244Val
ENST00000268124.11:c.730C>G MANE Select ENSP00000268124.5:p.Leu244Val
ENST00000530292.3:c.331C>G ENSP00000432885.2:p.Leu111Val
ENST00000635986.2:c.730C>G ENSP00000490653.2:p.Leu244Val
ENST00000636774.1:c.730C>G ENSP00000489799.1:p.Leu244Val
ENST00000666746.1:c.387C>G
ENST00000672071.1:n.928C>G
ENST00000268124.9:c.730C>G ENSP00000268124.5:p.Leu244Val
ENST00000442287.6:c.730C>G ENSP00000399851.2:p.Leu244Val
ENST00000631044.2:c.*113C>G ENSP00000486730.1:n.*113C>G
NM_001126131.1:c.730C>G NP_001119603.1:p.Leu244Val
NM_002693.2:c.730C>G NP_002684.1:p.Leu244Val
NM_001126131.2:c.730C>G NP_001119603.1:p.Leu244Val
NM_002693.3:c.730C>G MANE Select NP_002684.1:p.Leu244Val