Linked Data
ClinVar Variation Id:
317385
dbSNP Id:
rs566641514
ExAC:
15:90319773 G / A
gnomAD v2:
15-90319773-G-A
gnomAD v3:
15-89776542-G-A
gnomAD v4:
15-89776542-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.89776542G>A , CM000677.2:g.89776542G>A | GRCh38 |
| NC_000015.9:g.90319773G>A , CM000677.1:g.90319773G>A | GRCh37 |
| NC_000015.8:g.88120777G>A | NCBI36 |
| NG_008608.1:g.5185G>A | |
| NG_008608.2:g.20952G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341735.5:c.185G>A MANE Select | ENSP00000342392.3:p.Arg62Gln | |
| ENST00000341735.3:c.185G>A | ENSP00000342392.3:p.Arg62Gln | |
| ENST00000558723.1:n.39-1523G>A | ||
| ENST00000560219.2:c.31-1523G>A | ENSP00000452998.1:n.31-1523G>A | |
| NM_001039958.1:c.185G>A | NP_001035047.1:p.Arg62Gln | |
| NM_001039958.2:c.185G>A MANE Select | NP_001035047.1:p.Arg62Gln |