HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55125020_55125059del , CM000666.2:g.55125020_55125059del | GRCh38 |
NC_000004.11:g.55991187_55991226del , CM000666.1:g.55991187_55991226del | GRCh37 |
NC_000004.10:g.55685944_55685983del | NCBI36 |
NG_012004.1:g.5539_5578del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263923.5:c.67+170_67+209del MANE Select | ENSP00000263923.4:n.67+170_67+209del | |
ENST00000263923.4:c.67+170_67+209del | ENSP00000263923.4:n.67+170_67+209del | |
ENST00000512566.1:n.67+170_67+209del | ||
NM_002253.2:c.67+170_67+209del | NP_002244.1:n.67+170_67+209del | |
NM_002253.3:c.67+170_67+209del | NP_002244.1:n.67+170_67+209del | |
NM_002253.4:c.67+170_67+209del MANE Select | NP_002244.1:n.67+170_67+209del |