Linked Data
gnomAD v4:
20-46016511-C-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46016511C>G , CM000682.2:g.46016511C>G | GRCh38 |
| NC_000020.10:g.44645150C>G , CM000682.1:g.44645150C>G | GRCh37 |
| NC_000020.9:g.44078557C>G | NCBI36 |
| NG_011468.1:g.12604C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372330.3:c.*143C>G (MMP9) MANE Select | ENSP00000361405.3:n.*143C>G | |
| NM_004994.2:c.*143C>G (MMP9) | NP_004985.2:n.*143C>G | |
| NR_147699.1:n.669-1723G>C (SLC12A5-AS1) | ||
| NM_004994.3:c.*143C>G (MMP9) MANE Select | NP_004985.2:n.*143C>G |