Linked Data
ClinVar Variation Id:
495812
dbSNP Id:
rs1469347068
gnomAD v3:
10-87863552-G-A
gnomAD v4:
10-87863552-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.87863552G>A , CM000672.2:g.87863552G>A | GRCh38 |
| NC_000010.10:g.89623309G>A , CM000672.1:g.89623309G>A | GRCh37 |
| NC_000010.9:g.89613289G>A | NCBI36 |
| NG_007466.2:g.5115G>A , LRG_311:g.5115G>A | |
| NG_033079.1:g.4886C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706954.1:c.-16-902G>A | ENSP00000516674.1:n.-16-902G>A | |
| ENST00000688308.1:c.-17+439G>A | ENSP00000508752.1:n.-17+439G>A | |
| ENST00000693560.1:c.-398G>A | ENSP00000509861.1:n.-398G>A | |
| ENST00000371953.7:c.-918G>A | ENSP00000361021.3:n.-918G>A | |
| ENST00000610634.1:c.-1020G>A | ENSP00000477517.1:n.-1020G>A | |
| NM_000314.5:c.-917G>A | NP_000305.3:n.-917G>A | |
| NM_000314.6:c.-917G>A | NP_000305.3:n.-917G>A | |
| NM_001304717.2:c.-398G>A | NP_001291646.2:n.-398G>A | |
| NM_001304718.1:c.-1622G>A | NP_001291647.1:n.-1622G>A |