Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46016430_46016431delinsAG , CM000682.2:g.46016430_46016431delinsAG | GRCh38 |
| NC_000020.10:g.44645069_44645070delinsAG , CM000682.1:g.44645069_44645070delinsAG | GRCh37 |
| NC_000020.9:g.44078476_44078477delinsAG | NCBI36 |
| NG_011468.1:g.12523_12524delinsAG |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000372330.3:c.*62_*63delinsAG (MMP9) MANE Select | ENSP00000361405.3:n.*62_*63delinsAG | |
| NM_004994.2:c.*62_*63delinsAG (MMP9) | NP_004985.2:n.*62_*63delinsAG | |
| NR_147699.1:n.669-1643_669-1642delinsCT (SLC12A5-AS1) | ||
| NM_004994.3:c.*62_*63delinsAG (MMP9) MANE Select | NP_004985.2:n.*62_*63delinsAG |