HGVS | Genome Assembly |
---|---|
NC_000008.11:g.127343322T>C , CM000670.2:g.127343322T>C | GRCh38 |
NC_000008.10:g.128355568T>C , CM000670.1:g.128355568T>C | GRCh37 |
NC_000008.9:g.128424750T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000645438.1:c.-560+3887T>C (POU5F1B) | ENSP00000495779.1:n.-560+3887T>C | |
NR_117099.1:n.457+3887T>C (CASC21) | ||
NR_117100.1:n.1177-53262A>G (CASC8) |