Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102776323C>T , CM000673.2:g.102776323C>T | GRCh38 |
| NC_000011.9:g.102647054C>T , CM000673.1:g.102647054C>T | GRCh37 |
| NC_000011.8:g.102152264C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000279441.9:c.889G>A (MMP10) MANE Select | ENSP00000279441.4:p.Ala297Thr | |
| ENST00000279441.8:c.889G>A (MMP10) | ENSP00000279441.4:p.Ala297Thr | |
| ENST00000371455.7:n.325-21701C>T (WTAPP1) | ||
| NM_002425.2:c.889G>A (MMP10) | NP_002416.1:p.Ala297Thr | |
| NM_002425.3:c.889G>A (MMP10) MANE Select | NP_002416.1:p.Ala297Thr |