Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46016325T= , CM000682.2:g.46016325T= | GRCh38 |
| NC_000020.10:g.44644964T= , CM000682.1:g.44644964T= | GRCh37 |
| NC_000020.9:g.44078371T= | NCBI36 |
| NG_011468.1:g.12418T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000372330.3:c.2081T= (MMP9) MANE Select | ENSP00000361405.3:p.Val694= | |
| NM_004994.2:c.2081T= (MMP9) | NP_004985.2:p.Val694= | |
| NR_147699.1:n.669-1537A= (SLC12A5-AS1) | ||
| NM_004994.3:c.2081T= (MMP9) MANE Select | NP_004985.2:p.Val694= |