Linked Data
gnomAD v4:
20-46016492-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46016492C>A , CM000682.2:g.46016492C>A | GRCh38 |
| NC_000020.10:g.44645131C>A , CM000682.1:g.44645131C>A | GRCh37 |
| NC_000020.9:g.44078538C>A | NCBI36 |
| NG_011468.1:g.12585C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000372330.3:c.*124C>A (MMP9) MANE Select | ENSP00000361405.3:n.*124C>A | |
| NM_004994.2:c.*124C>A (MMP9) | NP_004985.2:n.*124C>A | |
| NR_147699.1:n.669-1704G>T (SLC12A5-AS1) | ||
| NM_004994.3:c.*124C>A (MMP9) MANE Select | NP_004985.2:n.*124C>A |