Linked Data
dbSNP Id:
rs1164843677
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.213985724C>G , CM000663.2:g.213985724C>G | GRCh38 |
| NC_000001.10:g.214159067C>G , CM000663.1:g.214159067C>G | GRCh37 |
| NC_000001.9:g.212225690C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000471129.1:c.-68+2401C>G (PROX1) | ENSP00000419517.1:n.-68+2401C>G | |
| NR_037850.2:n.85+345G>C (PROX1-AS1) | ||
| XM_011509773.1:c.-68+2401C>G (PROX1) | XP_011508075.1:n.-68+2401C>G | |
| XM_011509773.2:c.-68+2401C>G (PROX1) | XP_011508075.1:n.-68+2401C>G |