Linked Data
ClinVar Variation Id:
2085060
ClinVar RCV Id:
RCV002996084
dbSNP Id:
rs773914510
ExAC:
1:203681251 G / A
gnomAD v2:
1-203681251-G-A
gnomAD v4:
1-203712123-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.203712123G>A , CM000663.2:g.203712123G>A | GRCh38 |
| NC_000001.10:g.203681251G>A , CM000663.1:g.203681251G>A | GRCh37 |
| NC_000001.9:g.201947874G>A | NCBI36 |
| NG_029589.1:g.90337G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000341360.7:c.2195G>A | ENSP00000340930.2:p.Arg732His | |
| ENST00000705901.1:c.2159G>A | ENSP00000516177.1:p.Arg720His | |
| ENST00000357681.10:c.2195G>A MANE Select | ENSP00000350310.5:p.Arg732His | |
| ENST00000341360.6:c.2195G>A | ENSP00000340930.2:p.Arg732His | |
| ENST00000357681.9:c.2195G>A | ENSP00000350310.5:p.Arg732His | |
| ENST00000367218.7:c.2195G>A | ENSP00000356187.3:p.Arg732His | |
| NM_001001396.2:c.2195G>A | NP_001001396.1:p.Arg732His | |
| NM_001684.4:c.2195G>A | NP_001675.3:p.Arg732His | |
| NM_001365783.1:c.2195G>A | NP_001352712.1:p.Arg732His | |
| NM_001365784.1:c.2195G>A | NP_001352713.1:p.Arg732His | |
| NM_001365783.2:c.2195G>A | NP_001352712.1:p.Arg732His | |
| NM_001684.5:c.2195G>A MANE Select | NP_001675.3:p.Arg732His | |
| NM_001001396.3:c.2195G>A | NP_001001396.1:p.Arg732His | |
| NM_001365784.2:c.2195G>A | NP_001352713.1:p.Arg732His |