HGVS | Genome Assembly |
---|---|
NC_000021.9:g.44456784_44456786del , CM000683.2:g.44456784_44456786del | GRCh38 |
NC_000021.8:g.45876667_45876669del , CM000683.1:g.45876667_45876669del | GRCh37 |
NC_000021.7:g.44701095_44701097del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291592.6:c.140_142del MANE Select | ENSP00000291592.4:p.Ala47del | |
ENST00000291592.5:c.140_142del | ENSP00000291592.4:p.Ala47del | |
NM_030891.4:c.140_142del | NP_112153.1:p.Ala47del | |
NM_030891.5:c.140_142del | NP_112153.1:p.Ala47del | |
NM_030891.6:c.140_142del MANE Select | NP_112153.1:p.Ala47del |