HGVS | Genome Assembly |
---|---|
NC_000002.12:g.47376922del , CM000664.2:g.47376922del | GRCh38 |
NC_000002.11:g.47604061del , CM000664.1:g.47604061del | GRCh37 |
NC_000002.10:g.47457565del | NCBI36 |
NG_012352.2:g.36760del , LRG_215:g.36760del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263735.9:c.492-92del MANE Select | ENSP00000263735.4:n.492-92del | |
ENST00000263735.8:c.492-92del | ENSP00000263735.4:n.492-92del | |
ENST00000405271.5:c.576-92del | ENSP00000385476.1:n.576-92del | |
ENST00000456133.5:c.576-92del | ENSP00000410675.1:n.576-92del | |
ENST00000490733.1:n.341-92del | ||
NM_002354.2:c.492-92del , LRG_215t1:c.492-92del | NP_002345.2:n.492-92del | |
NM_002354.3:c.492-92del MANE Select | NP_002345.2:n.492-92del |