Linked Data
gnomAD v4:
20-1994225-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.1994225T>C , CM000682.2:g.1994225T>C | GRCh38 |
| NC_000020.10:g.1974871T>C , CM000682.1:g.1974871T>C | GRCh37 |
| NC_000020.9:g.1922871T>C | NCBI36 |
| NG_028027.1:g.5021A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000651882.1:c.-391A>G (PDYN) | ENSP00000498752.1:n.-391A>G | |
| ENST00000539905.5:c.-334A>G (PDYN) | ENSP00000440185.1:n.-334A>G | |
| NM_001190898.2:c.-391A>G (PDYN) | NP_001177827.1:n.-391A>G | |
| NM_001190899.2:c.-334A>G (PDYN) | NP_001177828.1:n.-334A>G | |
| NM_024411.4:c.-394A>G (PDYN) | NP_077722.1:n.-394A>G | |
| XR_244229.1:n.1217-12707T>C (PDYN-AS1) | ||
| NR_134520.1:n.1253-12707T>C (PDYN-AS1) |