Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46016277T>A , CM000682.2:g.46016277T>A | GRCh38 |
| NC_000020.10:g.44644916T>A , CM000682.1:g.44644916T>A | GRCh37 |
| NC_000020.9:g.44078323T>A | NCBI36 |
| NG_011468.1:g.12370T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372330.3:c.2033T>A (MMP9) MANE Select | ENSP00000361405.3:p.Phe678Tyr | |
| NM_004994.2:c.2033T>A (MMP9) | NP_004985.2:p.Phe678Tyr | |
| NR_147699.1:n.669-1489A>T (SLC12A5-AS1) | ||
| NM_004994.3:c.2033T>A (MMP9) MANE Select | NP_004985.2:p.Phe678Tyr |