gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.13830003 (EAS)
Genomes Max Group AF
0.13512162 (EAS)
Exomes Max Group AF
0.17729771 (EAS)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.112971371G>A , CM000674.2:g.112971371G>A | GRCh38 |
| NC_000012.11:g.113409176G>A , CM000674.1:g.113409176G>A | GRCh37 |
| NC_000012.10:g.111893559G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000228928.12:c.*1398G>A (OAS3) MANE Select | ENSP00000228928.7:n.*1398G>A | |
| ENST00000549918.2:n.2922G>A (OAS3) | ||
| ENST00000679354.1:c.*1398G>A (OAS3) | ENSP00000505880.1:n.*1398G>A | |
| ENST00000679483.1:c.*1398G>A (OAS3) | ENSP00000505798.1:n.*1398G>A | |
| ENST00000679493.1:c.*1237G>A (OAS3) | ENSP00000506397.1:n.*1237G>A | |
| ENST00000679505.1:c.*4319G>A (OAS3) | ENSP00000506118.1:n.*4319G>A | |
| ENST00000679517.1:c.*3937G>A (OAS3) | ENSP00000506294.1:n.*3937G>A | |
| ENST00000679547.1:c.*4085G>A (OAS3) | ENSP00000506567.1:n.*4085G>A | |
| ENST00000679562.1:c.*4160G>A (OAS3) | ENSP00000505418.1:n.*4160G>A | |
| ENST00000679812.1:c.*2923G>A (OAS3) | ENSP00000505154.1:n.*2923G>A | |
| ENST00000679912.1:c.*1835G>A (OAS3) | ENSP00000504871.1:n.*1835G>A | |
| ENST00000680044.1:c.*1398G>A (OAS3) | ENSP00000505627.1:n.*1398G>A | |
| ENST00000680090.1:c.*2342G>A (OAS3) | ENSP00000506611.1:n.*2342G>A | |
| ENST00000680177.1:c.*2923G>A (OAS3) | ENSP00000505925.1:n.*2923G>A | |
| ENST00000680293.1:c.*2888G>A (OAS3) | ENSP00000505651.1:n.*2888G>A | |
| ENST00000681002.1:c.*1736G>A (OAS3) | ENSP00000506106.1:n.*1736G>A | |
| ENST00000681134.1:c.*2002G>A (OAS3) | ENSP00000506146.1:n.*2002G>A | |
| ENST00000681346.1:c.*1412G>A (OAS3) | ENSP00000505939.1:n.*1412G>A | |
| ENST00000681497.1:c.*1398G>A (OAS3) | ENSP00000505225.1:n.*1398G>A | |
| ENST00000681764.1:c.*2342G>A (OAS3) | ENSP00000506335.1:n.*2342G>A | |
| ENST00000228928.11:c.*1398G>A (OAS3) | ENSP00000228928.7:n.*1398G>A | |
| NM_006187.3:c.*1398G>A (OAS3) | NP_006178.2:n.*1398G>A | |
| XM_005253889.2:c.*1398G>A (OAS3) | XP_005253946.1:n.*1398G>A | |
| XM_011538415.1:c.-2560G>A (OAS2) | XP_011536717.1:n.-2560G>A | |
| XM_005253889.4:c.*1398G>A (OAS3) | XP_005253946.1:n.*1398G>A | |
| XM_017019363.2:c.*1398G>A (OAS3) | XP_016874852.1:n.*1398G>A | |
| NM_006187.4:c.*1398G>A (OAS3) MANE Select | NP_006178.2:n.*1398G>A |