ClinVar Variation:
dbSNP:
gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00074445 (AFR)
Genomes Max Group AF
0.00078863 (AFR)
Exomes Max Group AF
0.00054341 (AFR)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.63957338C>A , CM000679.2:g.63957338C>A | GRCh38 |
| NC_000017.10:g.62034698C>A , CM000679.1:g.62034698C>A | GRCh37 |
| NC_000017.9:g.59388430C>A | NCBI36 |
| NG_011699.1:g.20581G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000435607.3:c.2200G>T MANE Select | ENSP00000396320.1:p.Ala734Ser | |
| ENST00000578147.5:c.2200G>T | ENSP00000463963.1:p.Ala734Ser | |
| NM_000334.4:c.2200G>T MANE Select | NP_000325.4:p.Ala734Ser | |
| XM_005257566.3:c.2200G>T | XP_005257623.1:p.Ala734Ser |