Linked Data
dbSNP Id:
rs778804889
ExAC:
22:42463801 A / C
gnomAD v2:
22-42463801-A-C
gnomAD v4:
22-42067797-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.42067797A>C , CM000684.2:g.42067797A>C | GRCh38 |
| NC_000022.10:g.42463801A>C , CM000684.1:g.42463801A>C | GRCh37 |
| NC_000022.9:g.40793747A>C | NCBI36 |
| NG_009247.1:g.8046T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000396398.8:c.292T>G MANE Select | ENSP00000379680.3:p.Phe98Val | |
| ENST00000396398.7:c.292T>G | ENSP00000379680.3:p.Phe98Val | |
| ENST00000402937.1:c.292T>G | ENSP00000384603.1:p.Phe98Val | |
| ENST00000403363.5:c.292T>G | ENSP00000385283.1:p.Phe98Val | |
| NM_000262.2:c.292T>G | NP_000253.1:p.Phe98Val | |
| XM_005261615.3:c.292T>G | XP_005261672.1:p.Phe98Val | |
| XM_005261616.3:c.292T>G | XP_005261673.1:p.Phe98Val | |
| NM_001362848.1:c.292T>G | NP_001349777.1:p.Phe98Val | |
| NM_001362850.1:c.292T>G | NP_001349779.1:p.Phe98Val | |
| NM_000262.3:c.292T>G MANE Select | NP_000253.1:p.Phe98Val |