Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46016464C>T , CM000682.2:g.46016464C>T | GRCh38 |
| NC_000020.10:g.44645103C>T , CM000682.1:g.44645103C>T | GRCh37 |
| NC_000020.9:g.44078510C>T | NCBI36 |
| NG_011468.1:g.12557C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004994.3:c.*96C>T (MMP9) MANE Select | NP_004985.2:n.*96C>T |
| ENST00000372330.3:c.*96C>T (MMP9) MANE Select | ENSP00000361405.3:n.*96C>T |
| NM_004994.2:c.*96C>T (MMP9) | NP_004985.2:n.*96C>T |
| NR_147699.1:n.669-1676G>A (SLC12A5-AS1) |