HGVS | Genome Assembly |
---|---|
NC_000017.11:g.7667753T= , CM000679.2:g.7667753T= | GRCh38 |
NC_000017.10:g.7571071T= , CM000679.1:g.7571071T= | GRCh37 |
NC_000017.9:g.7511796T= | NCBI36 |
NG_017013.2:g.24798A= , LRG_321:g.24798A= |
HGVS | Amino-acid Change |
---|---|
ENST00000359597.8:c.994-1509A= | ENSP00000352610.4:n.994-1509A= |
ENST00000413465.6:c.783-5739A= | ENSP00000410739.2:n.783-5739A= |
ENST00000635293.1:c.984-328A= | ENSP00000488924.1:n.984-328A= |