gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.000174 (NFE)
Genomes Max Group AF
0.00012401 (NFE)
Exomes Max Group AF
0.00017292 (NFE)
ClinVar Allele:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.90754937C>T , CM000677.2:g.90754937C>T | GRCh38 |
| NC_000015.9:g.91298167C>T , CM000677.1:g.91298167C>T | GRCh37 |
| NC_000015.8:g.89099171C>T | NCBI36 |
| NG_007272.1:g.42566C>T , LRG_20:g.42566C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000355112.8:c.1086C>T MANE Select | ENSP00000347232.3:p.Asp362= | |
| ENST00000648453.1:c.1086C>T | ENSP00000497646.1:p.Asp362= | |
| ENST00000680772.1:c.1086C>T | ENSP00000506117.1:p.Asp362= | |
| ENST00000681142.1:c.1086C>T | ENSP00000506682.1:p.Asp362= | |
| ENST00000355112.7:c.1086C>T | ENSP00000347232.3:p.Asp362= | |
| ENST00000558599.1:n.347C>T | ||
| ENST00000559724.5:c.1086C>T | ENSP00000453359.1:p.Asp362= | |
| ENST00000560509.5:c.1086C>T | ENSP00000454158.1:p.Asp362= | |
| NM_000057.3:c.1086C>T | NP_000048.1:p.Asp362= | |
| NM_001287246.1:c.1086C>T | NP_001274175.1:p.Asp362= | |
| NM_001287247.1:c.1086C>T | NP_001274176.1:p.Asp362= | |
| NM_001287248.1:c.-206C>T | NP_001274177.1:n.-206C>T | |
| XM_011521881.1:c.-96C>T | XP_011520183.1:n.-96C>T | |
| XM_011521882.1:c.1086C>T | XP_011520184.1:p.Asp362= | |
| XM_011521881.2:c.-96C>T | XP_011520183.1:n.-96C>T | |
| XM_011521882.3:c.1086C>T | XP_011520184.1:p.Asp362= | |
| NM_000057.4:c.1086C>T MANE Select | NP_000048.1:p.Asp362= | |
| NM_001287246.2:c.1086C>T | NP_001274175.1:p.Asp362= | |
| NM_001287247.2:c.1086C>T | NP_001274176.1:p.Asp362= | |
| NM_001287248.2:c.-206C>T | NP_001274177.1:n.-206C>T |