Linked Data
ClinVar Variation Id:
384209
dbSNP Id:
rs782336056
ExAC:
17:62492514 G / A
gnomAD v2:
17-62492514-G-A
gnomAD v3:
17-64496396-G-A
gnomAD v4:
17-64496396-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.64496396G>A , CM000679.2:g.64496396G>A | GRCh38 |
| NC_000017.10:g.62492514G>A , CM000679.1:g.62492514G>A | GRCh37 |
| NC_000017.9:g.59922976G>A | NCBI36 |
| NG_013029.1:g.5671C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000539111.7:c.562+11C>T (POLG2) MANE Select | ENSP00000442563.2:n.562+11C>T | |
| ENST00000585104.2:n.533+11C>T (POLG2) | ||
| ENST00000671755.1:c.533+11C>T (POLG2) | ||
| ENST00000673460.1:c.533+11C>T (POLG2) | ||
| ENST00000539111.6:c.562+11C>T (POLG2) | ENSP00000442563.2:n.562+11C>T | |
| ENST00000578997.1:c.224+136C>T (POLG2) | ENSP00000464389.1:n.224+136C>T | |
| ENST00000585141.5:n.613+11C>T (POLG2) | ||
| NM_007215.3:c.562+11C>T (POLG2) | NP_009146.2:n.562+11C>T | |
| XM_006721651.2:c.562+11C>T (POLG2) | XP_006721714.1:n.562+11C>T | |
| XR_243630.1:n.613+11C>T (POLG2) | ||
| XR_934357.1:n.613+11C>T (POLG2) | ||
| XR_934358.1:n.613+11C>T (POLG2) | ||
| XM_024450708.1:c.*104G>A (MILR1) | XP_024306476.1:n.*104G>A | |
| XR_002957990.1:n.1346G>A (MILR1) | ||
| NM_007215.4:c.562+11C>T (POLG2) MANE Select | NP_009146.2:n.562+11C>T |