HGVS | Genome Assembly |
---|---|
NC_000001.11:g.149927732del , CM000663.2:g.149927732del | GRCh38 |
NC_000001.10:g.149899624del , CM000663.1:g.149899624del | GRCh37 |
NC_000001.9:g.148166248del | NCBI36 |
NG_032777.1:g.5522del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271628.9:c.29del MANE Select | ENSP00000271628.8:p.Asn10IlefsTer30 | |
ENST00000271628.8:c.29del | ENSP00000271628.8:p.Asn10IlefsTer30 | |
NM_005850.4:c.29del | NP_005841.1:p.Asn10IlefsTer30 | |
NM_005850.5:c.29del MANE Select | NP_005841.1:p.Asn10IlefsTer30 |