Linked Data
ClinVar Variation Id:
129992
dbSNP Id:
rs144439703
ExAC:
15:89876722 G / A
gnomAD v2:
15-89876722-G-A
gnomAD v3:
15-89333491-G-A
gnomAD v4:
15-89333491-G-A
COSMIC:
COSM966312
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.89333491G>A , CM000677.2:g.89333491G>A | GRCh38 |
| NC_000015.9:g.89876722G>A , CM000677.1:g.89876722G>A | GRCh37 |
| NC_000015.8:g.87677726G>A | NCBI36 |
| NG_008218.1:g.6305C>T | |
| NG_008218.2:g.6305C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000636937.2:c.264C>T (POLG) | ENSP00000516154.1:p.Phe88= | |
| ENST00000706918.1:c.319C>T (POLGARF) | ENSP00000516626.1:p.Arg107Trp | |
| ENST00000268124.11:c.264C>T (POLG) MANE Select | ENSP00000268124.5:p.Phe88= | |
| ENST00000635986.2:c.264C>T (POLG) | ENSP00000490653.2:p.Phe88= | |
| ENST00000636774.1:c.264C>T (POLG) | ENSP00000489799.1:p.Phe88= | |
| ENST00000650303.2:c.319C>T (POLG) | ENSP00000497242.2:p.Arg107Trp | |
| ENST00000672071.1:n.462C>T (POLG) | ||
| ENST00000268124.9:c.264C>T (POLG) | ENSP00000268124.5:p.Phe88= | |
| ENST00000442287.6:c.264C>T (POLG) | ENSP00000399851.2:p.Phe88= | |
| ENST00000631044.2:c.264C>T (POLG) | ENSP00000486730.1:p.Phe88= | |
| NM_001126131.1:c.264C>T (POLG) | NP_001119603.1:p.Phe88= | |
| NM_002693.2:c.264C>T (POLG) | NP_002684.1:p.Phe88= | |
| NM_001126131.2:c.264C>T (POLG) | NP_001119603.1:p.Phe88= | |
| NM_002693.3:c.264C>T (POLG) MANE Select | NP_002684.1:p.Phe88= |