Linked Data
dbSNP Id:
rs778665464
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.181713102G>C , CM000665.2:g.181713102G>C | GRCh38 |
| NC_000003.11:g.181430890G>C , CM000665.1:g.181430890G>C | GRCh37 |
| NC_000003.10:g.182913584G>C | NCBI36 |
| NG_009080.1:g.6169G>C , LRG_719:g.6169G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000325404.3:c.742G>C (SOX2) MANE Select | ENSP00000323588.1:p.Ala248Pro | |
| ENST00000325404.2:c.742G>C (SOX2) | ENSP00000323588.1:p.Ala248Pro | |
| NM_003106.3:c.742G>C (SOX2) | NP_003097.1:p.Ala248Pro | |
| NR_004053.3:n.768-2083G>C (SOX2-OT) | ||
| NR_075089.1:n.767+13219G>C (SOX2-OT) | ||
| NR_075090.1:n.482-26467G>C (SOX2-OT) | ||
| NR_075091.1:n.783-2083G>C (SOX2-OT) | ||
| NR_075092.1:n.782+13219G>C (SOX2-OT) | ||
| NR_075093.1:n.473-26467G>C (SOX2-OT) | ||
| NM_003106.4:c.742G>C (SOX2) MANE Select | NP_003097.1:p.Ala248Pro |