Linked Data
dbSNP Id:
rs761957590
ExAC:
22:23627353 A / G
gnomAD v2:
22-23627353-A-G
gnomAD v4:
22-23285166-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.23285166A>G , CM000684.2:g.23285166A>G | GRCh38 |
| NC_000022.10:g.23627353A>G , CM000684.1:g.23627353A>G | GRCh37 |
| NC_000022.9:g.21957353A>G | NCBI36 |
| NG_009244.1:g.109802A>G | |
| NG_009244.2:g.109802A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000305877.13:c.2371A>G MANE Select | ENSP00000303507.8:p.Ile791Val | |
| ENST00000305877.12:c.2371A>G | ENSP00000303507.8:p.Ile791Val | |
| ENST00000359540.7:c.2371A>G | ENSP00000352535.3:p.Ile791Val | |
| ENST00000398512.9:c.1270-2978A>G | ENSP00000381524.6:n.1270-2978A>G | |
| ENST00000466076.1:n.445A>G | ||
| ENST00000487968.5:n.1024A>G | ||
| NM_004327.3:c.2371A>G | NP_004318.3:p.Ile791Val | |
| NM_021574.2:c.2371A>G | NP_067585.2:p.Ile791Val | |
| NM_004327.4:c.2371A>G MANE Select | NP_004318.3:p.Ile791Val | |
| NM_021574.3:c.2371A>G | NP_067585.2:p.Ile791Val |