Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.181713148C>T , CM000665.2:g.181713148C>T | GRCh38 |
| NC_000003.11:g.181430936C>T , CM000665.1:g.181430936C>T | GRCh37 |
| NC_000003.10:g.182913630C>T | NCBI36 |
| NG_009080.1:g.6215C>T , LRG_719:g.6215C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325404.3:c.788C>T (SOX2) MANE Select | ENSP00000323588.1:p.Ala263Val | |
| ENST00000325404.2:c.788C>T (SOX2) | ENSP00000323588.1:p.Ala263Val | |
| NM_003106.3:c.788C>T (SOX2) | NP_003097.1:p.Ala263Val | |
| NR_004053.3:n.768-2037C>T (SOX2-OT) | ||
| NR_075089.1:n.767+13265C>T (SOX2-OT) | ||
| NR_075090.1:n.482-26421C>T (SOX2-OT) | ||
| NR_075091.1:n.783-2037C>T (SOX2-OT) | ||
| NR_075092.1:n.782+13265C>T (SOX2-OT) | ||
| NR_075093.1:n.473-26421C>T (SOX2-OT) | ||
| NM_003106.4:c.788C>T (SOX2) MANE Select | NP_003097.1:p.Ala263Val |