HGVS | Genome Assembly |
---|---|
NC_000002.12:g.26135306_26135311del , CM000664.2:g.26135306_26135311del | GRCh38 |
NC_000002.11:g.26358175_26358180del , CM000664.1:g.26358175_26358180del | GRCh37 |
NC_000002.10:g.26211679_26211684del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264710.5:c.*285_*290del MANE Select | ENSP00000264710.4:n.*285_*290del | |
ENST00000264710.4:c.*285_*290del | ENSP00000264710.4:n.*285_*290del | |
ENST00000495146.5:n.1251_1256del | ||
NM_016131.4:c.*285_*290del | NP_057215.3:n.*285_*290del | |
XM_024452565.1:c.*285_*290del | XP_024308333.1:n.*285_*290del | |
NM_016131.5:c.*285_*290del MANE Select | NP_057215.3:n.*285_*290del |