HGVS | Genome Assembly |
---|---|
NC_000005.10:g.175441535_175441562del , CM000667.2:g.175441535_175441562del | GRCh38 |
NC_000005.9:g.174868538_174868565del , CM000667.1:g.174868538_174868565del | GRCh37 |
NC_000005.8:g.174801144_174801171del | NCBI36 |
NG_011802.1:g.7606_7633del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000393752.3:c.*204_*231del MANE Select | ENSP00000377353.1:n.*204_*231del | |
ENST00000393752.2:c.*204_*231del | ENSP00000377353.1:n.*204_*231del | |
NM_000794.3:c.*204_*231del | NP_000785.1:n.*204_*231del | |
NM_000794.4:c.*204_*231del | NP_000785.1:n.*204_*231del | |
NM_000794.5:c.*204_*231del MANE Select | NP_000785.1:n.*204_*231del |