Linked Data
ClinVar Variation Id:
756143
ClinVar RCV Id:
RCV000933617
dbSNP Id:
rs1596362738
gnomAD v4:
15-89333623-C-T
MyVariant Identifiers:
chr15:g.89876854C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.89333623C>T , CM000677.2:g.89333623C>T | GRCh38 |
| NC_000015.9:g.89876854C>T , CM000677.1:g.89876854C>T | GRCh37 |
| NC_000015.8:g.87677858C>T | NCBI36 |
| NG_008218.1:g.6173G>A | |
| NG_008218.2:g.6173G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000636937.2:c.132G>A (POLG) | ENSP00000516154.1:p.Gln44= | |
| ENST00000706918.1:c.187G>A (POLGARF) | ENSP00000516626.1:p.Ala63Thr | |
| ENST00000268124.11:c.132G>A (POLG) MANE Select | ENSP00000268124.5:p.Gln44= | |
| ENST00000635986.2:c.132G>A (POLG) | ENSP00000490653.2:p.Gln44= | |
| ENST00000636774.1:c.132G>A (POLG) | ENSP00000489799.1:p.Gln44= | |
| ENST00000650303.2:c.187G>A (POLG) | ENSP00000497242.2:p.Ala63Thr | |
| ENST00000672071.1:n.330G>A (POLG) | ||
| ENST00000268124.9:c.132G>A (POLG) | ENSP00000268124.5:p.Gln44= | |
| ENST00000442287.6:c.132G>A (POLG) | ENSP00000399851.2:p.Gln44= | |
| ENST00000631044.2:c.132G>A (POLG) | ENSP00000486730.1:p.Gln44= | |
| NM_001126131.1:c.132G>A (POLG) | NP_001119603.1:p.Gln44= | |
| NM_002693.2:c.132G>A (POLG) | NP_002684.1:p.Gln44= | |
| NM_001126131.2:c.132G>A (POLG) | NP_001119603.1:p.Gln44= | |
| NM_002693.3:c.132G>A (POLG) MANE Select | NP_002684.1:p.Gln44= |