Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.2803240G>C , CM000674.2:g.2803240G>C | GRCh38 |
| NC_000012.11:g.2912406G>C , CM000674.1:g.2912406G>C | GRCh37 |
| NC_000012.10:g.2782667G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000001008.6:c.1362G>C (FKBP4) MANE Select | ENSP00000001008.4:p.Gln454His | |
| ENST00000001008.5:c.1362G>C (FKBP4) | ENSP00000001008.4:p.Gln454His | |
| ENST00000544366.1:c.44G>C (FKBP4) | ||
| NM_002014.3:c.1362G>C (FKBP4) | NP_002005.1:p.Gln454His | |
| XM_011520929.1:c.1227G>C (FKBP4) | XP_011519231.1:p.Gln409His | |
| NR_146317.1:n.364-6294C>G (ITFG2-AS1) | ||
| XM_011520929.2:c.1227G>C (FKBP4) | XP_011519231.1:p.Gln409His | |
| NM_002014.4:c.1362G>C (FKBP4) MANE Select | NP_002005.1:p.Gln454His |