Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.1994215C>T , CM000682.2:g.1994215C>T | GRCh38 |
| NC_000020.10:g.1974861C>T , CM000682.1:g.1974861C>T | GRCh37 |
| NC_000020.9:g.1922861C>T | NCBI36 |
| NG_028027.1:g.5031G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000651882.1:c.-381G>A (PDYN) | ENSP00000498752.1:n.-381G>A | |
| ENST00000539905.5:c.-324G>A (PDYN) | ENSP00000440185.1:n.-324G>A | |
| NM_001190898.2:c.-381G>A (PDYN) | NP_001177827.1:n.-381G>A | |
| NM_001190899.2:c.-324G>A (PDYN) | NP_001177828.1:n.-324G>A | |
| NM_024411.4:c.-384G>A (PDYN) | NP_077722.1:n.-384G>A | |
| XR_244229.1:n.1217-12717C>T (PDYN-AS1) | ||
| NR_134520.1:n.1253-12717C>T (PDYN-AS1) |