HGVS | Genome Assembly |
---|---|
NC_000008.11:g.127343229A>G , CM000670.2:g.127343229A>G | GRCh38 |
NC_000008.10:g.128355475A>G , CM000670.1:g.128355475A>G | GRCh37 |
NC_000008.9:g.128424657A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000645438.1:c.-560+3794A>G (POU5F1B) | ENSP00000495779.1:n.-560+3794A>G | |
NR_117099.1:n.457+3794A>G (CASC21) | ||
NR_117100.1:n.1177-53169T>C (CASC8) |