Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102789832T>C , CM000673.2:g.102789832T>C | GRCh38 |
| NC_000011.9:g.102660563T>C , CM000673.1:g.102660563T>C | GRCh37 |
| NC_000011.8:g.102165773T>C | NCBI36 |
| NG_011740.1:g.13404A>G | |
| NG_011740.2:g.13404A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000680179.1:n.1168A>G (MMP1) | ||
| ENST00000681445.1:n.1164A>G (MMP1) | ||
| ENST00000681643.1:n.1190A>G (MMP1) | ||
| ENST00000371455.7:n.325-8192T>C (WTAPP1) | ||
| ENST00000525739.6:n.390-3313T>C (WTAPP1) | ||
| ENST00000544704.1:n.344+5768T>C (WTAPP1) | ||
| NR_038390.1:n.390-3313T>C (WTAPP1) |