HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160881859_160881865del , CM000663.2:g.160881859_160881865del | GRCh38 |
NC_000001.10:g.160851649_160851655del , CM000663.1:g.160851649_160851655del | GRCh37 |
NC_000001.9:g.159118273_159118279del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000326245.4:c.405+94_405+100del MANE Select | ENSP00000323587.3:n.405+94_405+100del | |
ENST00000326245.3:c.405+94_405+100del | ENSP00000323587.3:n.405+94_405+100del | |
ENST00000464077.1:n.339+94_339+100del | ||
NM_017625.2:c.405+94_405+100del | NP_060095.2:n.405+94_405+100del | |
NM_017625.3:c.405+94_405+100del MANE Select | NP_060095.2:n.405+94_405+100del |