HGVS | Genome Assembly |
---|---|
NC_000020.11:g.46016240T= , CM000682.2:g.46016240T= | GRCh38 |
NC_000020.10:g.44644879T= , CM000682.1:g.44644879T= | GRCh37 |
NC_000020.9:g.44078286T= | NCBI36 |
NG_011468.1:g.12333T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372330.3:c.2006-10T= (MMP9) MANE Select | ENSP00000361405.3:n.2006-10T= | |
NM_004994.2:c.2006-10T= (MMP9) | NP_004985.2:n.2006-10T= | |
NR_147699.1:n.669-1452A= (SLC12A5-AS1) | ||
NM_004994.3:c.2006-10T= (MMP9) MANE Select | NP_004985.2:n.2006-10T= |