Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.213985913T>C , CM000663.2:g.213985913T>C | GRCh38 |
| NC_000001.10:g.214159256T>C , CM000663.1:g.214159256T>C | GRCh37 |
| NC_000001.9:g.212225879T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NR_037850.2:n.85+156A>G (PROX1-AS1) | |
| ENST00000471129.1:c.-68+2590T>C (PROX1) | ENSP00000419517.1:n.-68+2590T>C |
| XM_011509773.1:c.-68+2590T>C (PROX1) | XP_011508075.1:n.-68+2590T>C |
| XM_011509773.2:c.-68+2590T>C (PROX1) | XP_011508075.1:n.-68+2590T>C |