HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55125536_55125538del , CM000666.2:g.55125536_55125538del | GRCh38 |
NC_000004.11:g.55991703_55991705del , CM000666.1:g.55991703_55991705del | GRCh37 |
NC_000004.10:g.55686460_55686462del | NCBI36 |
NG_012004.1:g.5059_5061del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263923.5:c.-244_-242del MANE Select | ENSP00000263923.4:n.-244_-242del | |
ENST00000263923.4:c.-244_-242del | ENSP00000263923.4:n.-244_-242del | |
NM_002253.2:c.-244_-242del | NP_002244.1:n.-244_-242del | |
NM_002253.3:c.-244_-242del | NP_002244.1:n.-244_-242del | |
NM_002253.4:c.-244_-242del MANE Select | NP_002244.1:n.-244_-242del |