Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.47416482C>T , CM000663.2:g.47416482C>T | GRCh38 |
| NC_000001.10:g.47882154C>T , CM000663.1:g.47882154C>T | GRCh37 |
| NC_000001.9:g.47654741C>T | NCBI36 |
| NG_016192.1:g.5411C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000335071.4:c.167C>T (FOXE3) MANE Select | ENSP00000334472.2:p.Ala56Val | |
| ENST00000335071.3:c.167C>T (FOXE3) | ENSP00000334472.2:p.Ala56Val | |
| NM_012186.2:c.167C>T (FOXE3) | NP_036318.1:p.Ala56Val | |
| NR_126355.1:n.29-6581G>A (LINC01389) | ||
| NM_012186.3:c.167C>T (FOXE3) MANE Select | NP_036318.1:p.Ala56Val |