Canonical Allele Identifier: CA7725151
Gene: POLG HGNC NCBI
POLGARF HGNC NCBI

Linked Data

dbSNP Id: rs139134661

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89333511C>G , CM000677.2:g.89333511C>G GRCh38
NC_000015.9:g.89876742C>G , CM000677.1:g.89876742C>G GRCh37
NC_000015.8:g.87677746C>G NCBI36
NG_008218.1:g.6285G>C
NG_008218.2:g.6285G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.244G>C (POLG) ENSP00000516154.1:p.Gly82Arg
ENST00000706918.1:c.299G>C (POLGARF) ENSP00000516626.1:p.Arg100Thr
ENST00000268124.11:c.244G>C (POLG) MANE Select ENSP00000268124.5:p.Gly82Arg
ENST00000635986.2:c.244G>C (POLG) ENSP00000490653.2:p.Gly82Arg
ENST00000636774.1:c.244G>C (POLG) ENSP00000489799.1:p.Gly82Arg
ENST00000650303.2:c.299G>C (POLG) ENSP00000497242.2:p.Arg100Thr
ENST00000672071.1:n.442G>C (POLG)
ENST00000268124.9:c.244G>C (POLG) ENSP00000268124.5:p.Gly82Arg
ENST00000442287.6:c.244G>C (POLG) ENSP00000399851.2:p.Gly82Arg
ENST00000631044.2:c.244G>C (POLG) ENSP00000486730.1:p.Gly82Arg
NM_001126131.1:c.244G>C (POLG) NP_001119603.1:p.Gly82Arg
NM_002693.2:c.244G>C (POLG) NP_002684.1:p.Gly82Arg
NM_001126131.2:c.244G>C (POLG) NP_001119603.1:p.Gly82Arg
NM_002693.3:c.244G>C (POLG) MANE Select NP_002684.1:p.Gly82Arg