Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.2799139G>A , CM000674.2:g.2799139G>A | GRCh38 |
| NC_000012.11:g.2908305G>A , CM000674.1:g.2908305G>A | GRCh37 |
| NC_000012.10:g.2778566G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000001008.6:c.566G>A (FKBP4) MANE Select | ENSP00000001008.4:p.Arg189His | |
| ENST00000001008.5:c.566G>A (FKBP4) | ENSP00000001008.4:p.Arg189His | |
| ENST00000543037.1:n.373G>A (FKBP4) | ||
| NM_002014.3:c.566G>A (FKBP4) | NP_002005.1:p.Arg189His | |
| XM_011520929.1:c.431G>A (FKBP4) | XP_011519231.1:p.Arg144His | |
| NR_146317.1:n.364-2193C>T (ITFG2-AS1) | ||
| XM_011520929.2:c.431G>A (FKBP4) | XP_011519231.1:p.Arg144His | |
| NM_002014.4:c.566G>A (FKBP4) MANE Select | NP_002005.1:p.Arg189His |