HGVS | Genome Assembly |
---|---|
NC_000020.11:g.46016325T>C , CM000682.2:g.46016325T>C | GRCh38 |
NC_000020.10:g.44644964T>C , CM000682.1:g.44644964T>C | GRCh37 |
NC_000020.9:g.44078371T>C | NCBI36 |
NG_011468.1:g.12418T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000372330.3:c.2081T>C (MMP9) MANE Select | ENSP00000361405.3:p.Val694Ala | |
NM_004994.2:c.2081T>C (MMP9) | NP_004985.2:p.Val694Ala | |
NR_147699.1:n.669-1537A>G (SLC12A5-AS1) | ||
NM_004994.3:c.2081T>C (MMP9) MANE Select | NP_004985.2:p.Val694Ala |