HGVS | Genome Assembly |
---|---|
NC_000001.11:g.213985935A>G , CM000663.2:g.213985935A>G | GRCh38 |
NC_000001.10:g.214159278A>G , CM000663.1:g.214159278A>G | GRCh37 |
NC_000001.9:g.212225901A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000471129.1:c.-68+2612A>G (PROX1) | ENSP00000419517.1:n.-68+2612A>G | |
NR_037850.2:n.85+134T>C (PROX1-AS1) | ||
XM_011509773.1:c.-68+2612A>G (PROX1) | XP_011508075.1:n.-68+2612A>G | |
XM_011509773.2:c.-68+2612A>G (PROX1) | XP_011508075.1:n.-68+2612A>G |