HGVS | Genome Assembly |
---|---|
NC_000008.11:g.127343289T>A , CM000670.2:g.127343289T>A | GRCh38 |
NC_000008.10:g.128355535T>A , CM000670.1:g.128355535T>A | GRCh37 |
NC_000008.9:g.128424717T>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000645438.1:c.-560+3854T>A (POU5F1B) | ENSP00000495779.1:n.-560+3854T>A | |
NR_117099.1:n.457+3854T>A (CASC21) | ||
NR_117100.1:n.1177-53229A>T (CASC8) |