HGVS | Genome Assembly |
---|---|
NC_000015.10:g.74749516_74749519del , CM000677.2:g.74749516_74749519del | GRCh38 |
NC_000015.9:g.75041857_75041860del , CM000677.1:g.75041857_75041860del | GRCh37 |
NC_000015.8:g.72828910_72828913del | NCBI36 |
NG_008431.1:g.31975_31978del | |
NG_008431.2:g.31975_31978del | |
NG_061543.1:g.5672_5675del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000343932.5:c.-9-214_-9-211del MANE Select | ENSP00000342007.4:n.-9-214_-9-211del | |
ENST00000343932.4:c.-9-214_-9-211del | ENSP00000342007.4:n.-9-214_-9-211del | |
NM_000761.4:c.-9-214_-9-211del | NP_000752.2:n.-9-214_-9-211del | |
NM_000761.5:c.-9-214_-9-211del MANE Select | NP_000752.2:n.-9-214_-9-211del |