HGVS | Genome Assembly |
---|---|
NC_000001.11:g.213985671G>A , CM000663.2:g.213985671G>A | GRCh38 |
NC_000001.10:g.214159014G>A , CM000663.1:g.214159014G>A | GRCh37 |
NC_000001.9:g.212225637G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000471129.1:c.-68+2348G>A (PROX1) | ENSP00000419517.1:n.-68+2348G>A | |
NR_037850.2:n.85+398C>T (PROX1-AS1) | ||
XM_011509773.1:c.-68+2348G>A (PROX1) | XP_011508075.1:n.-68+2348G>A | |
XM_011509773.2:c.-68+2348G>A (PROX1) | XP_011508075.1:n.-68+2348G>A |