dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.125591814A>C , CM000673.2:g.125591814A>C | GRCh38 |
| NC_000011.9:g.125461709A>C , CM000673.1:g.125461709A>C | GRCh37 |
| NC_000011.8:g.124966919A>C | NCBI36 |
| NG_042806.1:g.4020A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000530526.1:n.151+604T>G (STT3A-AS1) | ||
| ENST00000648911.1:c.-259+604T>G (FEZ1) | ENSP00000497070.1:n.-259+604T>G | |
| ENST00000527606.5:c.-109A>C (STT3A) | ENSP00000436558.1:n.-109A>C | |
| NR_132372.1:n.151+604T>G (STT3A-AS1) | ||
| XR_948139.1:n.218+604T>G (STT3A-AS1) |