Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.181713716T>A , CM000665.2:g.181713716T>A | GRCh38 |
| NC_000003.11:g.181431504T>A , CM000665.1:g.181431504T>A | GRCh37 |
| NC_000003.10:g.182914198T>A | NCBI36 |
| NG_009080.1:g.6783T>A , LRG_719:g.6783T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003106.4:c.*402T>A (SOX2) MANE Select | NP_003097.1:n.*402T>A |
| ENST00000325404.3:c.*402T>A (SOX2) MANE Select | ENSP00000323588.1:n.*402T>A |
| NM_003106.3:c.*402T>A (SOX2) | NP_003097.1:n.*402T>A |
| NR_004053.3:n.768-1469T>A (SOX2-OT) | |
| NR_075089.1:n.767+13833T>A (SOX2-OT) | |
| NR_075090.1:n.482-25853T>A (SOX2-OT) | |
| NR_075091.1:n.783-1469T>A (SOX2-OT) | |
| NR_075092.1:n.782+13833T>A (SOX2-OT) | |
| NR_075093.1:n.473-25853T>A (SOX2-OT) | |
| ENST00000325404.2:c.*402T>A (SOX2) | ENSP00000323588.1:n.*402T>A |