Linked Data
gnomAD v4:
10-87863546-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87863546C>A , CM000672.2:g.87863546C>A | GRCh38 |
| NC_000010.10:g.89623303C>A , CM000672.1:g.89623303C>A | GRCh37 |
| NC_000010.9:g.89613283C>A | NCBI36 |
| NG_007466.2:g.5109C>A , LRG_311:g.5109C>A | |
| NG_033079.1:g.4892G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706954.1:c.-17+904C>A | ENSP00000516674.1:n.-17+904C>A | |
| ENST00000688308.1:c.-17+433C>A | ENSP00000508752.1:n.-17+433C>A | |
| ENST00000693560.1:c.-404C>A | ENSP00000509861.1:n.-404C>A | |
| ENST00000371953.7:c.-924C>A | ENSP00000361021.3:n.-924C>A | |
| ENST00000610634.1:c.-1026C>A | ENSP00000477517.1:n.-1026C>A | |
| NM_000314.5:c.-923C>A | NP_000305.3:n.-923C>A | |
| NM_000314.6:c.-923C>A | NP_000305.3:n.-923C>A | |
| NM_001304717.2:c.-404C>A | NP_001291646.2:n.-404C>A | |
| NM_001304718.1:c.-1628C>A | NP_001291647.1:n.-1628C>A |