HGVS | Genome Assembly |
---|---|
NC_000012.12:g.15322293G>A , CM000674.2:g.15322293G>A | GRCh38 |
NC_000012.11:g.15475227G>A , CM000674.1:g.15475227G>A | GRCh37 |
NC_000012.10:g.15366494G>A | NCBI36 |
NG_031857.1:g.5037G>A |
HGVS | Amino-acid Change |
---|---|
NM_002848.3:c.-434G>A (PTPRO) | NP_002839.1:n.-434G>A |
NM_030667.2:c.-434G>A (PTPRO) | NP_109592.1:n.-434G>A |
ENST00000393736.3:c.-115+15084C>T (RERG) | ENSP00000440887.1:n.-115+15084C>T |
ENST00000674316.1:c.-434G>A (PTPRO) | ENSP00000501352.1:n.-434G>A |
XR_931384.1:n.329+15084C>T | |
XR_931386.1:n.329+15084C>T | |
XR_931387.1:n.329+15084C>T |