Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.213985934T= , CM000663.2:g.213985934T= | GRCh38 |
| NC_000001.10:g.214159277T= , CM000663.1:g.214159277T= | GRCh37 |
| NC_000001.9:g.212225900T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000471129.1:c.-68+2611T= (PROX1) | ENSP00000419517.1:n.-68+2611T= | |
| NR_037850.2:n.85+135A= (PROX1-AS1) | ||
| XM_011509773.1:c.-68+2611T= (PROX1) | XP_011508075.1:n.-68+2611T= | |
| XM_011509773.2:c.-68+2611T= (PROX1) | XP_011508075.1:n.-68+2611T= |