HGVS | Genome Assembly |
---|---|
NC_000018.10:g.60371566del , CM000680.2:g.60371566del | GRCh38 |
NC_000018.9:g.58038799del , CM000680.1:g.58038799del | GRCh37 |
NC_000018.8:g.56189779del | NCBI36 |
NG_016441.1:g.6204del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299766.5:c.785del MANE Select | ENSP00000299766.3:p.Phe262SerfsTer4 | |
ENST00000299766.4:c.785del | ENSP00000299766.3:p.Phe262SerfsTer4 | |
NM_005912.2:c.785del | NP_005903.2:p.Phe262SerfsTer4 | |
NM_005912.3:c.785del MANE Select | NP_005903.2:p.Phe262SerfsTer4 |