Linked Data
gnomAD v4:
12-52516752-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.52516752C>T , CM000674.2:g.52516752C>T | GRCh38 |
| NC_000012.11:g.52910536C>T , CM000674.1:g.52910536C>T | GRCh37 |
| NC_000012.10:g.51196803C>T | NCBI36 |
| NG_008297.1:g.8708G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000252242.9:c.1324G>A MANE Select | ENSP00000252242.4:p.Ala442Thr | |
| ENST00000252242.8:c.1324G>A | ENSP00000252242.4:p.Ala442Thr | |
| ENST00000547890.5:n.702G>A | ||
| ENST00000548409.5:c.446G>A | ||
| ENST00000549511.5:n.531G>A | ||
| ENST00000552629.5:n.1422G>A | ||
| NM_000424.3:c.1324G>A | NP_000415.2:p.Ala442Thr | |
| NM_000424.4:c.1324G>A MANE Select | NP_000415.2:p.Ala442Thr |