HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73323212del , CM000677.2:g.73323212del | GRCh38 |
NC_000015.9:g.73615553del , CM000677.1:g.73615553del | GRCh37 |
NC_000015.8:g.71402606del | NCBI36 |
NG_009063.1:g.51057del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.2885del MANE Select | ENSP00000261917.3:p.Pro962HisfsTer23 | |
ENST00000261917.3:c.2885del | ENSP00000261917.3:p.Pro962HisfsTer23 | |
NM_005477.2:c.2885del | NP_005468.1:p.Pro962HisfsTer23 | |
XM_011521148.1:c.1667del | XP_011519450.1:p.Pro556HisfsTer23 | |
XM_011521148.2:c.1667del | XP_011519450.1:p.Pro556HisfsTer23 | |
NM_005477.3:c.2885del MANE Select | NP_005468.1:p.Pro962HisfsTer23 |