HGVS | Genome Assembly |
---|---|
NC_000017.11:g.7668323T= , CM000679.2:g.7668323T= | GRCh38 |
NC_000017.10:g.7571641T= , CM000679.1:g.7571641T= | GRCh37 |
NC_000017.9:g.7512366T= | NCBI36 |
NG_017013.2:g.24228A= , LRG_321:g.24228A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000359597.8:c.994-2079A= | ENSP00000352610.4:n.994-2079A= | |
ENST00000413465.6:c.782+5858A= | ENSP00000410739.2:n.782+5858A= | |
ENST00000635293.1:c.984-898A= | ENSP00000488924.1:n.984-898A= |