HGVS | Genome Assembly |
---|---|
NC_000007.14:g.150992770_150992771del , CM000669.2:g.150992770_150992771del | GRCh38 |
NC_000007.13:g.150689858_150689859del , CM000669.1:g.150689858_150689859del | GRCh37 |
NC_000007.12:g.150320791_150320792del | NCBI36 |
NG_011992.1:g.6712_6713del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000297494.8:c.-51-983_-51-982del MANE Select | ENSP00000297494.3:n.-51-983_-51-982del | |
ENST00000297494.7:c.-51-983_-51-982del | ENSP00000297494.3:n.-51-983_-51-982del | |
ENST00000461406.5:c.-149+1470_-149+1471del | ENSP00000417143.1:n.-149+1470_-149+1471del | |
NM_000603.4:c.-51-983_-51-982del | NP_000594.2:n.-51-983_-51-982del | |
NM_000603.5:c.-51-983_-51-982del MANE Select | NP_000594.2:n.-51-983_-51-982del |