Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.1994232C>A , CM000682.2:g.1994232C>A | GRCh38 |
| NC_000020.10:g.1974878C>A , CM000682.1:g.1974878C>A | GRCh37 |
| NC_000020.9:g.1922878C>A | NCBI36 |
| NG_028027.1:g.5014G>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000651882.1:c.-398G>T (PDYN) | ENSP00000498752.1:n.-398G>T | |
| ENST00000539905.5:c.-341G>T (PDYN) | ENSP00000440185.1:n.-341G>T | |
| NM_001190898.2:c.-398G>T (PDYN) | NP_001177827.1:n.-398G>T | |
| NM_001190899.2:c.-341G>T (PDYN) | NP_001177828.1:n.-341G>T | |
| NM_024411.4:c.-401G>T (PDYN) | NP_077722.1:n.-401G>T | |
| XR_244229.1:n.1217-12700C>A (PDYN-AS1) | ||
| NR_134520.1:n.1253-12700C>A (PDYN-AS1) |