HGVS | Genome Assembly |
---|---|
NC_000008.11:g.127343152A>T , CM000670.2:g.127343152A>T | GRCh38 |
NC_000008.10:g.128355398A>T , CM000670.1:g.128355398A>T | GRCh37 |
NC_000008.9:g.128424580A>T | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000645438.1:c.-560+3717A>T (POU5F1B) | ENSP00000495779.1:n.-560+3717A>T | |
NR_117099.1:n.457+3717A>T (CASC21) | ||
NR_117100.1:n.1177-53092T>A (CASC8) |