Canonical Allele Identifier: CA972593291
Gene: POLG HGNC NCBI

Linked Data

dbSNP Id: rs2055347360

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89318786T>C , CM000677.2:g.89318786T>C GRCh38
NC_000015.9:g.89862017T>C , CM000677.1:g.89862017T>C GRCh37
NC_000015.8:g.87663021T>C NCBI36
NG_008218.1:g.21010A>G
NG_011736.1:g.79824T>C , LRG_500:g.79824T>C
NG_008218.2:g.21010A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.3274-37A>G ENSP00000516154.1:n.3274-37A>G
ENST00000268124.11:c.3274-37A>G MANE Select ENSP00000268124.5:n.3274-37A>G
ENST00000530292.3:c.2875-37A>G ENSP00000432885.2:n.2875-37A>G
ENST00000635986.2:c.*344-37A>G ENSP00000490653.2:n.*344-37A>G
ENST00000636774.1:c.*1841-37A>G ENSP00000489799.1:n.*1841-37A>G
ENST00000637238.1:c.2083-37A>G ENSP00000490756.1:n.2083-37A>G
ENST00000637264.1:c.2346-37A>G
ENST00000666746.1:c.2851-37A>G
ENST00000672071.1:n.3472-37A>G
ENST00000672695.1:n.451-37A>G
ENST00000672923.2:n.3274-37A>G
ENST00000268124.9:c.3274-37A>G ENSP00000268124.5:n.3274-37A>G
ENST00000442287.6:c.3274-37A>G ENSP00000399851.2:n.3274-37A>G
ENST00000530292.2:c.358-37A>G ENSP00000432885.1:n.358-37A>G
ENST00000631044.2:c.*2698-37A>G ENSP00000486730.1:n.*2698-37A>G
NM_001126131.1:c.3274-37A>G NP_001119603.1:n.3274-37A>G
NM_002693.2:c.3274-37A>G NP_002684.1:n.3274-37A>G
NM_001126131.2:c.3274-37A>G NP_001119603.1:n.3274-37A>G
NM_002693.3:c.3274-37A>G MANE Select NP_002684.1:n.3274-37A>G