Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.47416226G>T , CM000663.2:g.47416226G>T | GRCh38 |
| NC_000001.10:g.47881898G>T , CM000663.1:g.47881898G>T | GRCh37 |
| NC_000001.9:g.47654485G>T | NCBI36 |
| NG_016192.1:g.5155G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_012186.2:c.-90G>T (FOXE3) | NP_036318.1:n.-90G>T |
| NR_126355.1:n.29-6325C>A (LINC01389) | |
| ENST00000335071.3:c.-90G>T (FOXE3) | ENSP00000334472.2:n.-90G>T |