Canonical Allele Identifier: CA7724177
Gene: POLG HGNC NCBI

Linked Data

dbSNP Id: rs753096283

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89318788C>G , CM000677.2:g.89318788C>G GRCh38
NC_000015.9:g.89862019C>G , CM000677.1:g.89862019C>G GRCh37
NC_000015.8:g.87663023C>G NCBI36
NG_008218.1:g.21008G>C
NG_011736.1:g.79826C>G , LRG_500:g.79826C>G
NG_008218.2:g.21008G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.3274-39G>C ENSP00000516154.1:n.3274-39G>C
ENST00000268124.11:c.3274-39G>C MANE Select ENSP00000268124.5:n.3274-39G>C
ENST00000530292.3:c.2875-39G>C ENSP00000432885.2:n.2875-39G>C
ENST00000635986.2:c.*344-39G>C ENSP00000490653.2:n.*344-39G>C
ENST00000636774.1:c.*1841-39G>C ENSP00000489799.1:n.*1841-39G>C
ENST00000637238.1:c.2083-39G>C ENSP00000490756.1:n.2083-39G>C
ENST00000637264.1:c.2346-39G>C
ENST00000666746.1:c.2851-39G>C
ENST00000672071.1:n.3472-39G>C
ENST00000672695.1:n.451-39G>C
ENST00000672923.2:n.3274-39G>C
ENST00000268124.9:c.3274-39G>C ENSP00000268124.5:n.3274-39G>C
ENST00000442287.6:c.3274-39G>C ENSP00000399851.2:n.3274-39G>C
ENST00000530292.2:c.358-39G>C ENSP00000432885.1:n.358-39G>C
ENST00000631044.2:c.*2698-39G>C ENSP00000486730.1:n.*2698-39G>C
NM_001126131.1:c.3274-39G>C NP_001119603.1:n.3274-39G>C
NM_002693.2:c.3274-39G>C NP_002684.1:n.3274-39G>C
NM_001126131.2:c.3274-39G>C NP_001119603.1:n.3274-39G>C
NM_002693.3:c.3274-39G>C MANE Select NP_002684.1:n.3274-39G>C