Linked Data
gnomAD v4:
11-102789841-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.102789841C>A , CM000673.2:g.102789841C>A | GRCh38 |
| NC_000011.9:g.102660572C>A , CM000673.1:g.102660572C>A | GRCh37 |
| NC_000011.8:g.102165782C>A | NCBI36 |
| NG_011740.1:g.13395G>T | |
| NG_011740.2:g.13395G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000680179.1:n.1159G>T (MMP1) | ||
| ENST00000681445.1:n.1155G>T (MMP1) | ||
| ENST00000681643.1:n.1181G>T (MMP1) | ||
| ENST00000371455.7:n.325-8183C>A (WTAPP1) | ||
| ENST00000525739.6:n.390-3304C>A (WTAPP1) | ||
| ENST00000544704.1:n.344+5777C>A (WTAPP1) | ||
| NR_038390.1:n.390-3304C>A (WTAPP1) |