HGVS | Genome Assembly |
---|---|
NC_000001.11:g.192811749del , CM000663.2:g.192811749del | GRCh38 |
NC_000001.10:g.192780879del , CM000663.1:g.192780879del | GRCh37 |
NC_000001.9:g.191047502del | NCBI36 |
NG_012800.1:g.7711del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000235382.7:c.*153del MANE Select | ENSP00000235382.5:n.*153del | |
ENST00000235382.6:c.*153del | ENSP00000235382.5:n.*153del | |
NM_002923.3:c.*153del | NP_002914.1:n.*153del | |
NM_002923.4:c.*153del MANE Select | NP_002914.1:n.*153del |