HGVS | Genome Assembly |
---|---|
NC_000024.10:g.22329563T>C , CM000686.2:g.22329563T>C | GRCh38 |
NC_000024.9:g.24475710T>C , CM000686.1:g.24475710T>C | GRCh37 |
NC_000024.8:g.22885098T>C | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000414629.6:c.-5+20593T>C | ENSP00000405745.2:n.-5+20593T>C | |
ENST00000445779.6:c.-5+20593T>C | ENSP00000389621.2:n.-5+20593T>C |