HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215817276_215817280del , CM000663.2:g.215817276_215817280del | GRCh38 |
NC_000001.10:g.215990618_215990622del , CM000663.1:g.215990618_215990622del | GRCh37 |
NC_000001.9:g.214057241_214057245del | NCBI36 |
NG_009497.1:g.611117_611121del | |
NG_009497.2:g.611169_611173del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.9372-85_9372-81del MANE Select | ENSP00000305941.3:n.9372-85_9372-81del | |
ENST00000674083.1:c.9372-85_9372-81del | ENSP00000501296.1:n.9372-85_9372-81del | |
ENST00000307340.7:c.9372-85_9372-81del | ENSP00000305941.3:n.9372-85_9372-81del | |
NM_206933.2:c.9372-85_9372-81del | NP_996816.2:n.9372-85_9372-81del | |
NM_206933.3:c.9372-85_9372-81del | NP_996816.2:n.9372-85_9372-81del | |
NM_206933.4:c.9372-85_9372-81del MANE Select | NP_996816.3:n.9372-85_9372-81del |