gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.89999652 (AFR)
Genomes Max Group AF
0.89506654 (AFR)
Exomes Max Group AF
0.90085252 (AFR)
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.128911444T>C , CM000673.2:g.128911444T>C | GRCh38 |
| NC_000011.9:g.128781339T>C , CM000673.1:g.128781339T>C | GRCh37 |
| NC_000011.8:g.128286549T>C | NCBI36 |
| NG_023406.2:g.25027T>C , LRG_333:g.25027T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000529694.6:c.171T>C MANE Select | ENSP00000433295.1:p.Ser57= | |
| ENST00000338350.4:c.171T>C | ENSP00000339960.4:p.Ser57= | |
| ENST00000529694.5:c.171T>C | ENSP00000433295.1:p.Ser57= | |
| ENST00000533599.1:c.171T>C | ENSP00000434266.1:p.Ser57= | |
| NM_000890.3:c.171T>C , LRG_333t1:c.171T>C | NP_000881.3:p.Ser57= | |
| XM_011542809.1:c.171T>C | XP_011541111.1:p.Ser57= | |
| XM_011542810.1:c.171T>C | XP_011541112.1:p.Ser57= | |
| NM_000890.4:c.171T>C | NP_000881.3:p.Ser57= | |
| NM_001354169.1:c.171T>C | NP_001341098.1:p.Ser57= | |
| XM_011542809.2:c.171T>C | XP_011541111.1:p.Ser57= | |
| XM_011542810.3:c.171T>C | XP_011541112.1:p.Ser57= | |
| NM_000890.5:c.171T>C MANE Select | NP_000881.3:p.Ser57= | |
| NM_001354169.2:c.171T>C | NP_001341098.1:p.Ser57= |