Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.64048840G>A , CM000682.2:g.64048840G>A | GRCh38 |
| NC_000020.10:g.62680193G>A , CM000682.1:g.62680193G>A | GRCh37 |
| NC_000020.9:g.62150637G>A | NCBI36 |
| NG_008095.1:g.5787C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340356.9:c.481C>T (SOX18) MANE Select | ENSP00000341815.7:p.Gln161Ter | |
| ENST00000340356.8:c.481C>T (SOX18) | ENSP00000341815.7:p.Gln161Ter | |
| NM_018419.2:c.481C>T (SOX18) | NP_060889.1:p.Gln161Ter | |
| XM_011529022.1:c.-2320+6445G>A (TCEA2) | XP_011527324.1:n.-2320+6445G>A | |
| XM_011529025.1:c.-2236+6445G>A (TCEA2) | XP_011527327.1:n.-2236+6445G>A | |
| XM_024451978.1:c.-2236+6445G>A (TCEA2) | XP_024307746.1:n.-2236+6445G>A | |
| NM_018419.3:c.481C>T (SOX18) MANE Select | NP_060889.1:p.Gln161Ter |