Canonical Allele Identifier: CA393772179
Gene: POLG HGNC NCBI
POLGARF HGNC NCBI

Linked Data

ClinVar Variation Id: 589825
ClinVar RCV Id: RCV002317538
dbSNP Id: rs866985804

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.89333378C>T , CM000677.2:g.89333378C>T GRCh38
NC_000015.9:g.89876609C>T , CM000677.1:g.89876609C>T GRCh37
NC_000015.8:g.87677613C>T NCBI36
NG_008218.1:g.6418G>A
NG_008218.2:g.6418G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000636937.2:c.377G>A (POLG) ENSP00000516154.1:p.Arg126His
ENST00000706918.1:c.432G>A (POLGARF) ENSP00000516626.1:p.Ala144=
ENST00000268124.11:c.377G>A (POLG) MANE Select ENSP00000268124.5:p.Arg126His
ENST00000635986.2:c.377G>A (POLG) ENSP00000490653.2:p.Arg126His
ENST00000636774.1:c.377G>A (POLG) ENSP00000489799.1:p.Arg126His
ENST00000650303.2:c.432G>A (POLG) ENSP00000497242.2:p.Ala144=
ENST00000666746.1:c.34G>A (POLG)
ENST00000672071.1:n.575G>A (POLG)
ENST00000268124.9:c.377G>A (POLG) ENSP00000268124.5:p.Arg126His
ENST00000442287.6:c.377G>A (POLG) ENSP00000399851.2:p.Arg126His
ENST00000631044.2:c.377G>A (POLG) ENSP00000486730.1:p.Arg126His
NM_001126131.1:c.377G>A (POLG) NP_001119603.1:p.Arg126His
NM_002693.2:c.377G>A (POLG) NP_002684.1:p.Arg126His
NM_001126131.2:c.377G>A (POLG) NP_001119603.1:p.Arg126His
NM_002693.3:c.377G>A (POLG) MANE Select NP_002684.1:p.Arg126His