gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.29623116 (AMR)
Genomes Max Group AF
0.29326347 (AMR)
Exomes Max Group AF
0.36643981 (AMR)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.35607710G>A , CM000668.2:g.35607710G>A | GRCh38 |
| NC_000006.11:g.35575487G>A , CM000668.1:g.35575487G>A | GRCh37 |
| NC_000006.10:g.35683465G>A | NCBI36 |
| NG_012645.2:g.125874C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357266.9:c.509-10306C>T (FKBP5) MANE Select | ENSP00000349811.3:n.509-10306C>T | |
| ENST00000357266.8:c.509-10306C>T (FKBP5) | ENSP00000349811.3:n.509-10306C>T | |
| ENST00000407266.1:n.83G>A (RPL36P9) | ||
| ENST00000536438.5:c.509-10306C>T (FKBP5) | ENSP00000444810.1:n.509-10306C>T | |
| ENST00000539068.5:c.509-10306C>T (FKBP5) | ENSP00000441205.1:n.509-10306C>T | |
| ENST00000542713.1:c.509-10306C>T (FKBP5) | ENSP00000442340.1:n.509-10306C>T | |
| NM_001145775.2:c.509-10306C>T (FKBP5) | NP_001139247.1:n.509-10306C>T | |
| NM_001145776.1:c.509-10306C>T (FKBP5) | NP_001139248.1:n.509-10306C>T | |
| NM_001145777.1:c.509-10306C>T (FKBP5) | NP_001139249.1:n.509-10306C>T | |
| NM_004117.3:c.509-10306C>T (FKBP5) | NP_004108.1:n.509-10306C>T | |
| XR_926744.1:n.1936+5387G>A | ||
| XR_002956345.1:n.1482+5387G>A | ||
| NM_001145775.3:c.509-10306C>T (FKBP5) | NP_001139247.1:n.509-10306C>T | |
| NM_001145776.2:c.509-10306C>T (FKBP5) | NP_001139248.1:n.509-10306C>T | |
| NM_001145777.2:c.509-10306C>T (FKBP5) | NP_001139249.1:n.509-10306C>T | |
| NM_004117.4:c.509-10306C>T (FKBP5) MANE Select | NP_004108.1:n.509-10306C>T |