HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114713995del , CM000663.2:g.114713995del | GRCh38 |
NC_000001.10:g.115256616del , CM000663.1:g.115256616del | GRCh37 |
NC_000001.9:g.115058139del | NCBI36 |
NG_007572.1:g.7900del , LRG_92:g.7900del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.112-17del MANE Select | ENSP00000358548.4:n.112-17del | |
ENST00000369535.4:c.112-17del | ENSP00000358548.4:n.112-17del | |
NM_002524.4:c.112-17del | NP_002515.1:n.112-17del | |
NM_002524.5:c.112-17del MANE Select | NP_002515.1:n.112-17del |