HGVS | Genome Assembly |
---|---|
NC_000005.10:g.175441641_175441643del , CM000667.2:g.175441641_175441643del | GRCh38 |
NC_000005.9:g.174868644_174868646del , CM000667.1:g.174868644_174868646del | GRCh37 |
NC_000005.8:g.174801250_174801252del | NCBI36 |
NG_011802.1:g.7523_7525del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000393752.3:c.*121_*123del MANE Select | ENSP00000377353.1:n.*121_*123del | |
ENST00000393752.2:c.*121_*123del | ENSP00000377353.1:n.*121_*123del | |
NM_000794.3:c.*121_*123del | NP_000785.1:n.*121_*123del | |
NM_000794.4:c.*121_*123del | NP_000785.1:n.*121_*123del | |
NM_000794.5:c.*121_*123del MANE Select | NP_000785.1:n.*121_*123del |