HGVS | Genome Assembly |
---|---|
NC_000020.11:g.46016358C>G , CM000682.2:g.46016358C>G | GRCh38 |
NC_000020.10:g.44644997C>G , CM000682.1:g.44644997C>G | GRCh37 |
NC_000020.9:g.44078404C>G | NCBI36 |
NG_011468.1:g.12451C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372330.3:c.2114C>G (MMP9) MANE Select | ENSP00000361405.3:p.Pro705Arg | |
NM_004994.2:c.2114C>G (MMP9) | NP_004985.2:p.Pro705Arg | |
NR_147699.1:n.669-1570G>C (SLC12A5-AS1) | ||
NM_004994.3:c.2114C>G (MMP9) MANE Select | NP_004985.2:p.Pro705Arg |