Linked Data
MyVariant Identifiers:
chr20:g.44644977C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46016338C>T , CM000682.2:g.46016338C>T | GRCh38 |
| NC_000020.10:g.44644977C>T , CM000682.1:g.44644977C>T | GRCh37 |
| NC_000020.9:g.44078384C>T | NCBI36 |
| NG_011468.1:g.12431C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000372330.3:c.2094C>T (MMP9) MANE Select | ENSP00000361405.3:p.Thr698= | |
| NM_004994.2:c.2094C>T (MMP9) | NP_004985.2:p.Thr698= | |
| NR_147699.1:n.669-1550G>A (SLC12A5-AS1) | ||
| NM_004994.3:c.2094C>T (MMP9) MANE Select | NP_004985.2:p.Thr698= |