Canonical Allele Identifier: CA716886866
Gene: POLG HGNC NCBI

Linked Data

dbSNP Id: rs147218850

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89323130A>T , CM000677.2:g.89323130A>T GRCh38
NC_000015.9:g.89866361A>T , CM000677.1:g.89866361A>T GRCh37
NC_000015.8:g.87667365A>T NCBI36
NG_008218.1:g.16666T>A
NG_008218.2:g.16666T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.2266-228T>A ENSP00000516154.1:n.2266-228T>A
ENST00000268124.11:c.2266-228T>A MANE Select ENSP00000268124.5:n.2266-228T>A
ENST00000530292.3:c.1867-228T>A ENSP00000432885.2:n.1867-228T>A
ENST00000635986.2:c.2266-228T>A ENSP00000490653.2:n.2266-228T>A
ENST00000636774.1:c.*833-228T>A ENSP00000489799.1:n.*833-228T>A
ENST00000637238.1:c.963-228T>A ENSP00000490756.1:n.963-228T>A
ENST00000637264.1:c.1338-228T>A
ENST00000666746.1:c.1843-228T>A
ENST00000670281.1:c.586-228T>A ENSP00000499709.1:n.586-228T>A
ENST00000672071.1:n.2464-228T>A
ENST00000672923.2:n.2368+274T>A
ENST00000268124.9:c.2266-228T>A ENSP00000268124.5:n.2266-228T>A
ENST00000442287.6:c.2266-228T>A ENSP00000399851.2:n.2266-228T>A
ENST00000526314.2:c.540-228T>A
ENST00000526398.1:c.415-228T>A
ENST00000528881.2:c.35-228T>A
ENST00000530715.5:c.25-228T>A ENSP00000431395.1:n.25-228T>A
ENST00000532584.5:n.467+274T>A
ENST00000631044.2:c.*1690-228T>A ENSP00000486730.1:n.*1690-228T>A
NM_001126131.1:c.2266-228T>A NP_001119603.1:n.2266-228T>A
NM_002693.2:c.2266-228T>A NP_002684.1:n.2266-228T>A
NM_001126131.2:c.2266-228T>A NP_001119603.1:n.2266-228T>A
NM_002693.3:c.2266-228T>A MANE Select NP_002684.1:n.2266-228T>A