Linked Data
gnomAD v4:
17-42909276-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42909276C>A , CM000679.2:g.42909276C>A | GRCh38 |
| NC_000017.10:g.41061293C>A , CM000679.1:g.41061293C>A | GRCh37 |
| NC_000017.9:g.38314819C>A | NCBI36 |
| NG_011808.1:g.13479C>A , LRG_147:g.13479C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000253801.7:c.447-27C>A MANE Select | ENSP00000253801.1:n.447-27C>A | |
| ENST00000253801.6:c.447-27C>A | ENSP00000253801.1:n.447-27C>A | |
| ENST00000585489.1:c.447-1639C>A | ENSP00000466202.1:n.447-1639C>A | |
| ENST00000592383.5:c.370-27C>A | ENSP00000465958.1:n.370-27C>A | |
| NM_000151.3:c.447-27C>A | NP_000142.2:n.447-27C>A | |
| NM_001270397.1:c.370-27C>A | NP_001257326.1:n.370-27C>A | |
| NM_000151.4:c.447-27C>A MANE Select | NP_000142.2:n.447-27C>A | |
| NM_001270397.2:c.370-27C>A | NP_001257326.1:n.370-27C>A |