Linked Data
gnomAD v4:
20-1994230-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.1994230T>G , CM000682.2:g.1994230T>G | GRCh38 |
| NC_000020.10:g.1974876T>G , CM000682.1:g.1974876T>G | GRCh37 |
| NC_000020.9:g.1922876T>G | NCBI36 |
| NG_028027.1:g.5016A>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000651882.1:c.-396A>C (PDYN) | ENSP00000498752.1:n.-396A>C | |
| ENST00000539905.5:c.-339A>C (PDYN) | ENSP00000440185.1:n.-339A>C | |
| NM_001190898.2:c.-396A>C (PDYN) | NP_001177827.1:n.-396A>C | |
| NM_001190899.2:c.-339A>C (PDYN) | NP_001177828.1:n.-339A>C | |
| NM_024411.4:c.-399A>C (PDYN) | NP_077722.1:n.-399A>C | |
| XR_244229.1:n.1217-12702T>G (PDYN-AS1) | ||
| NR_134520.1:n.1253-12702T>G (PDYN-AS1) |