HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215817296_215817301del , CM000663.2:g.215817296_215817301del | GRCh38 |
NC_000001.10:g.215990638_215990643del , CM000663.1:g.215990638_215990643del | GRCh37 |
NC_000001.9:g.214057261_214057266del | NCBI36 |
NG_009497.1:g.611103_611108del | |
NG_009497.2:g.611155_611160del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.9372-99_9372-94del MANE Select | ENSP00000305941.3:n.9372-99_9372-94del | |
ENST00000674083.1:c.9372-99_9372-94del | ENSP00000501296.1:n.9372-99_9372-94del | |
ENST00000307340.7:c.9372-99_9372-94del | ENSP00000305941.3:n.9372-99_9372-94del | |
NM_206933.2:c.9372-99_9372-94del | NP_996816.2:n.9372-99_9372-94del | |
NM_206933.3:c.9372-99_9372-94del | NP_996816.2:n.9372-99_9372-94del | |
NM_206933.4:c.9372-99_9372-94del MANE Select | NP_996816.3:n.9372-99_9372-94del |