Linked Data
gnomAD v4:
20-1994237-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.1994237C>T , CM000682.2:g.1994237C>T | GRCh38 |
| NC_000020.10:g.1974883C>T , CM000682.1:g.1974883C>T | GRCh37 |
| NC_000020.9:g.1922883C>T | NCBI36 |
| NG_028027.1:g.5009G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651882.1:c.-403G>A (PDYN) | ENSP00000498752.1:n.-403G>A | |
| ENST00000539905.5:c.-346G>A (PDYN) | ENSP00000440185.1:n.-346G>A | |
| NM_001190898.2:c.-403G>A (PDYN) | NP_001177827.1:n.-403G>A | |
| NM_001190899.2:c.-346G>A (PDYN) | NP_001177828.1:n.-346G>A | |
| NM_024411.4:c.-406G>A (PDYN) | NP_077722.1:n.-406G>A | |
| XR_244229.1:n.1217-12695C>T (PDYN-AS1) | ||
| NR_134520.1:n.1253-12695C>T (PDYN-AS1) |