Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.127343200A>G , CM000670.2:g.127343200A>G | GRCh38 |
| NC_000008.10:g.128355446A>G , CM000670.1:g.128355446A>G | GRCh37 |
| NC_000008.9:g.128424628A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645438.1:c.-560+3765A>G (POU5F1B) | ENSP00000495779.1:n.-560+3765A>G | |
| NR_117099.1:n.457+3765A>G (CASC21) | ||
| NR_117100.1:n.1177-53140T>C (CASC8) |