Canonical Allele Identifier: CA393773654
Gene: POLG HGNC NCBI
POLGARF HGNC NCBI

Linked Data

dbSNP Id: rs1171419088

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89333552T>C , CM000677.2:g.89333552T>C GRCh38
NC_000015.9:g.89876783T>C , CM000677.1:g.89876783T>C GRCh37
NC_000015.8:g.87677787T>C NCBI36
NG_008218.1:g.6244A>G
NG_008218.2:g.6244A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.203A>G (POLG) ENSP00000516154.1:p.Gln68Arg
ENST00000706918.1:c.258A>G (POLGARF) ENSP00000516626.1:p.Ala86=
ENST00000268124.11:c.203A>G (POLG) MANE Select ENSP00000268124.5:p.Gln68Arg
ENST00000635986.2:c.203A>G (POLG) ENSP00000490653.2:p.Gln68Arg
ENST00000636774.1:c.203A>G (POLG) ENSP00000489799.1:p.Gln68Arg
ENST00000650303.2:c.258A>G (POLG) ENSP00000497242.2:p.Ala86=
ENST00000672071.1:n.401A>G (POLG)
ENST00000268124.9:c.203A>G (POLG) ENSP00000268124.5:p.Gln68Arg
ENST00000442287.6:c.203A>G (POLG) ENSP00000399851.2:p.Gln68Arg
ENST00000631044.2:c.203A>G (POLG) ENSP00000486730.1:p.Gln68Arg
NM_001126131.1:c.203A>G (POLG) NP_001119603.1:p.Gln68Arg
NM_002693.2:c.203A>G (POLG) NP_002684.1:p.Gln68Arg
NM_001126131.2:c.203A>G (POLG) NP_001119603.1:p.Gln68Arg
NM_002693.3:c.203A>G (POLG) MANE Select NP_002684.1:p.Gln68Arg