| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.10005695A>G , CM000682.2:g.10005695A>G | GRCh38 |
| NC_000020.10:g.9986343A>G , CM000682.1:g.9986343A>G | GRCh37 |
| NC_000020.9:g.9934343A>G | NCBI36 |
| HGVS | Amino-acid Change |
|---|---|
| NR_109861.1:n.188-818A>G (PARAL1) | |
| ENST00000437504.1:n.394+19176A>G (ANKEF1) |