HGVS | Genome Assembly |
---|---|
NC_000005.10:g.148827306_148827308del , CM000667.2:g.148827306_148827308del | GRCh38 |
NC_000005.9:g.148206869_148206871del , CM000667.1:g.148206869_148206871del | GRCh37 |
NC_000005.8:g.148187062_148187064del | NCBI36 |
NG_016421.1:g.5714_5716del | |
NG_016421.2:g.5714_5716del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000305988.6:c.475_477del MANE Select | ENSP00000305372.4:p.Ile159del | |
ENST00000305988.5:c.475_477del | ENSP00000305372.4:p.Ile159del | |
NM_000024.5:c.475_477del | NP_000015.1:p.Ile159del | |
NM_000024.6:c.475_477del MANE Select | NP_000015.2:p.Ile159del |