Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.1994242A= , CM000682.2:g.1994242A= | GRCh38 |
| NC_000020.10:g.1974888A= , CM000682.1:g.1974888A= | GRCh37 |
| NC_000020.9:g.1922888A= | NCBI36 |
| NG_028027.1:g.5004T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651882.1:c.-408T= (PDYN) | ENSP00000498752.1:n.-408T= | |
| ENST00000539905.5:c.-351T= (PDYN) | ENSP00000440185.1:n.-351T= | |
| NM_001190898.2:c.-408T= (PDYN) | NP_001177827.1:n.-408T= | |
| NM_001190899.2:c.-351T= (PDYN) | NP_001177828.1:n.-351T= | |
| NM_024411.4:c.-411T= (PDYN) | NP_077722.1:n.-411T= | |
| XR_244229.1:n.1217-12690A= (PDYN-AS1) | ||
| NR_134520.1:n.1253-12690A= (PDYN-AS1) |