Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46016514T= , CM000682.2:g.46016514T= | GRCh38 |
| NC_000020.10:g.44645153T= , CM000682.1:g.44645153T= | GRCh37 |
| NC_000020.9:g.44078560T= | NCBI36 |
| NG_011468.1:g.12607T= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_004994.3:c.*146T= (MMP9) MANE Select | NP_004985.2:n.*146T= |
| ENST00000372330.3:c.*146T= (MMP9) MANE Select | ENSP00000361405.3:n.*146T= |
| NM_004994.2:c.*146T= (MMP9) | NP_004985.2:n.*146T= |
| NR_147699.1:n.669-1726A= (SLC12A5-AS1) |