HGVS | Genome Assembly |
---|---|
NC_000023.11:g.83508734del , CM000685.2:g.83508734del | GRCh38 |
NC_000023.10:g.82763742del , CM000685.1:g.82763742del | GRCh37 |
NC_000023.9:g.82650398del | NCBI36 |
NG_009936.2:g.5474del |
HGVS | Amino-acid Change |
---|---|
NM_000307.5:c.410del MANE Select | NP_000298.3:p.Pro137LeufsTer5 |
ENST00000644024.2:c.410del MANE Select | ENSP00000495996.1:p.Pro137LeufsTer5 |
NM_000307.4:c.410del | NP_000298.3:p.Pro137LeufsTer5 |
ENST00000373200.4:c.410del | ENSP00000362296.2:p.Pro137LeufsTer5 |