Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.181713069C>G , CM000665.2:g.181713069C>G | GRCh38 |
| NC_000003.11:g.181430857C>G , CM000665.1:g.181430857C>G | GRCh37 |
| NC_000003.10:g.182913551C>G | NCBI36 |
| NG_009080.1:g.6136C>G , LRG_719:g.6136C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325404.3:c.709C>G (SOX2) MANE Select | ENSP00000323588.1:p.Leu237Val | |
| ENST00000325404.2:c.709C>G (SOX2) | ENSP00000323588.1:p.Leu237Val | |
| NM_003106.3:c.709C>G (SOX2) | NP_003097.1:p.Leu237Val | |
| NR_004053.3:n.768-2116C>G (SOX2-OT) | ||
| NR_075089.1:n.767+13186C>G (SOX2-OT) | ||
| NR_075090.1:n.482-26500C>G (SOX2-OT) | ||
| NR_075091.1:n.783-2116C>G (SOX2-OT) | ||
| NR_075092.1:n.782+13186C>G (SOX2-OT) | ||
| NR_075093.1:n.473-26500C>G (SOX2-OT) | ||
| NM_003106.4:c.709C>G (SOX2) MANE Select | NP_003097.1:p.Leu237Val |