gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.00012791 (AMR)
Genomes Max Group AF
0.00030628 (AMR)
Exomes Max Group AF
0.00003174 (NFE)
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.791990G>A , CM000673.2:g.791990G>A | GRCh38 |
| NC_000011.9:g.791990G>A , CM000673.1:g.791990G>A | GRCh37 |
| NC_000011.8:g.781990G>A | NCBI36 |
| NG_023407.1:g.11280C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000628067.3:c.897C>T MANE Select | ENSP00000486058.1:p.Phe299= | |
| ENST00000320230.9:c.897C>T | ENSP00000322020.5:p.Phe299= | |
| ENST00000531214.5:c.897C>T | ENSP00000437236.1:p.Phe299= | |
| ENST00000628067.2:c.897C>T | ENSP00000486058.1:p.Phe299= | |
| NM_001191060.1:c.897C>T | NP_001177989.1:p.Phe299= | |
| NM_001191061.1:c.897C>T | NP_001177990.1:p.Phe299= | |
| NM_024698.5:c.897C>T | NP_078974.1:p.Phe299= | |
| XM_011520369.1:c.897C>T | XP_011518671.1:p.Phe299= | |
| XM_011520370.1:c.897C>T | XP_011518672.1:p.Phe299= | |
| XM_011520371.1:c.897C>T | XP_011518673.1:p.Phe299= | |
| XM_011520370.2:c.897C>T | XP_011518672.1:p.Phe299= | |
| XM_011520371.2:c.897C>T | XP_011518673.1:p.Phe299= | |
| XM_024448687.1:c.897C>T | XP_024304455.1:p.Phe299= | |
| XM_024448688.1:c.897C>T | XP_024304456.1:p.Phe299= | |
| XM_024448689.1:c.897C>T | XP_024304457.1:p.Phe299= | |
| NM_001191061.2:c.897C>T MANE Select | NP_001177990.1:p.Phe299= | |
| NM_024698.6:c.897C>T | NP_078974.1:p.Phe299= | |
| NM_001191060.2:c.897C>T | NP_001177989.1:p.Phe299= |