Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.127328627T>C , CM000670.2:g.127328627T>C | GRCh38 |
| NC_000008.10:g.128340872T>C , CM000670.1:g.128340872T>C | GRCh37 |
| NC_000008.9:g.128410054T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000645438.1:c.-715+6401T>C (POU5F1B) | ENSP00000495779.1:n.-715+6401T>C | |
| NR_117099.1:n.302+6401T>C (CASC21) | ||
| NR_117100.1:n.1177-38567A>G (CASC8) |