Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102836608C>T , CM000673.2:g.102836608C>T | GRCh38 |
| NC_000011.9:g.102707339C>T , CM000673.1:g.102707339C>T | GRCh37 |
| NC_000011.8:g.102212549C>T | NCBI36 |
| NG_012100.1:g.12004G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_002422.5:c.1334-382G>A (MMP3) MANE Select | NP_002413.1:n.1334-382G>A |
| ENST00000299855.10:c.1334-382G>A (MMP3) MANE Select | ENSP00000299855.5:n.1334-382G>A |
| NM_002422.3:c.1334-382G>A (MMP3) | NP_002413.1:n.1334-382G>A |
| NM_002422.4:c.1334-382G>A (MMP3) | NP_002413.1:n.1334-382G>A |
| NR_038390.1:n.2484C>T (WTAPP1) | |
| ENST00000299855.9:c.1334-382G>A (MMP3) | ENSP00000299855.5:n.1334-382G>A |
| ENST00000434103.1:c.265-80G>A (MMP3) | |
| ENST00000525739.6:n.2484C>T (WTAPP1) |