HGVS | Genome Assembly |
---|---|
NC_000020.11:g.46016470G>T , CM000682.2:g.46016470G>T | GRCh38 |
NC_000020.10:g.44645109G>T , CM000682.1:g.44645109G>T | GRCh37 |
NC_000020.9:g.44078516G>T | NCBI36 |
NG_011468.1:g.12563G>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372330.3:c.*102G>T (MMP9) MANE Select | ENSP00000361405.3:n.*102G>T | |
NM_004994.2:c.*102G>T (MMP9) | NP_004985.2:n.*102G>T | |
NR_147699.1:n.669-1682C>A (SLC12A5-AS1) | ||
NM_004994.3:c.*102G>T (MMP9) MANE Select | NP_004985.2:n.*102G>T |