HGVS | Genome Assembly |
---|---|
NC_000001.11:g.160881821_160881825dup , CM000663.2:g.160881821_160881825dup | GRCh38 |
NC_000001.10:g.160851611_160851615dup , CM000663.1:g.160851611_160851615dup | GRCh37 |
NC_000001.9:g.159118235_159118239dup | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000326245.4:c.405+148_405+152dup MANE Select | ENSP00000323587.3:n.405+148_405+152dup | |
ENST00000326245.3:c.405+148_405+152dup | ENSP00000323587.3:n.405+148_405+152dup | |
ENST00000464077.1:n.339+148_339+152dup | ||
NM_017625.2:c.405+148_405+152dup | NP_060095.2:n.405+148_405+152dup | |
NM_017625.3:c.405+148_405+152dup MANE Select | NP_060095.2:n.405+148_405+152dup |