Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.127401003T>A , CM000670.2:g.127401003T>A | GRCh38 |
| NC_000008.10:g.128413248T>A , CM000670.1:g.128413248T>A | GRCh37 |
| NC_000008.9:g.128482430T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000645438.1:c.-559-13885T>A (POU5F1B) | ENSP00000495779.1:n.-559-13885T>A | |
| NR_109834.1:n.605T>A (CCAT2) | ||
| NR_117100.1:n.1176+19826A>T (CASC8) |