Linked Data
dbSNP Id:
rs1857969979
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102789739C>G , CM000673.2:g.102789739C>G | GRCh38 |
| NC_000011.9:g.102660470C>G , CM000673.1:g.102660470C>G | GRCh37 |
| NC_000011.8:g.102165680C>G | NCBI36 |
| NG_011740.1:g.13497G>C | |
| NG_011740.2:g.13497G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000680179.1:n.1261G>C (MMP1) | ||
| ENST00000681445.1:n.1257G>C (MMP1) | ||
| ENST00000681643.1:n.1283G>C (MMP1) | ||
| ENST00000371455.7:n.325-8285C>G (WTAPP1) | ||
| ENST00000525739.6:n.390-3406C>G (WTAPP1) | ||
| ENST00000544704.1:n.344+5675C>G (WTAPP1) | ||
| NR_038390.1:n.390-3406C>G (WTAPP1) |