Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102798189T>C , CM000673.2:g.102798189T>C | GRCh38 |
| NC_000011.9:g.102668920T>C , CM000673.1:g.102668920T>C | GRCh37 |
| NC_000011.8:g.102174130T>C | NCBI36 |
| NG_011740.1:g.5047A>G | |
| NG_011740.2:g.5047A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371455.7:n.423+67T>C (WTAPP1) | ||
| ENST00000525739.6:n.682+67T>C (WTAPP1) | ||
| ENST00000544704.1:n.443+67T>C (WTAPP1) | ||
| NM_001145938.1:c.-143A>G (MMP1) | NP_001139410.1:n.-143A>G | |
| NM_002421.3:c.-97A>G (MMP1) | NP_002412.1:n.-97A>G | |
| NR_038390.1:n.682+67T>C (WTAPP1) |