HGVS | Genome Assembly |
---|---|
NC_000004.12:g.55112700_55112701del , CM000666.2:g.55112700_55112701del | GRCh38 |
NC_000004.11:g.55978867_55978868del , CM000666.1:g.55978867_55978868del | GRCh37 |
NC_000004.10:g.55673624_55673625del | NCBI36 |
NG_012004.1:g.17899_17900del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263923.5:c.976+607_976+608del MANE Select | ENSP00000263923.4:n.976+607_976+608del | |
ENST00000647068.1:n.989+607_989+608del | ||
ENST00000263923.4:c.976+607_976+608del | ENSP00000263923.4:n.976+607_976+608del | |
ENST00000512566.1:n.976+607_976+608del | ||
NM_002253.2:c.976+607_976+608del | NP_002244.1:n.976+607_976+608del | |
NM_002253.3:c.976+607_976+608del | NP_002244.1:n.976+607_976+608del | |
NM_002253.4:c.976+607_976+608del MANE Select | NP_002244.1:n.976+607_976+608del |