HGVS | Genome Assembly |
---|---|
NC_000008.11:g.127414148G>A , CM000670.2:g.127414148G>A | GRCh38 |
NC_000008.10:g.128426393G>A , CM000670.1:g.128426393G>A | GRCh37 |
NC_000008.9:g.128495575G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000465342.4:c.-559-740G>A (POU5F1B) | ENSP00000419298.2:n.-559-740G>A | |
ENST00000645438.1:c.-559-740G>A (POU5F1B) | ENSP00000495779.1:n.-559-740G>A | |
NR_117100.1:n.1176+6681C>T (CASC8) | ||
NM_001395745.1:c.-1299G>A (POU5F1B) | NP_001382674.1:n.-1299G>A |