HGVS | Genome Assembly |
---|---|
NC_000020.11:g.46016443G>A , CM000682.2:g.46016443G>A | GRCh38 |
NC_000020.10:g.44645082G>A , CM000682.1:g.44645082G>A | GRCh37 |
NC_000020.9:g.44078489G>A | NCBI36 |
NG_011468.1:g.12536G>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000372330.3:c.*75G>A (MMP9) MANE Select | ENSP00000361405.3:n.*75G>A | |
NM_004994.2:c.*75G>A (MMP9) | NP_004985.2:n.*75G>A | |
NR_147699.1:n.669-1655C>T (SLC12A5-AS1) | ||
NM_004994.3:c.*75G>A (MMP9) MANE Select | NP_004985.2:n.*75G>A |