HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114713984_114713985del , CM000663.2:g.114713984_114713985del | GRCh38 |
NC_000001.10:g.115256605_115256606del , CM000663.1:g.115256605_115256606del | GRCh37 |
NC_000001.9:g.115058128_115058129del | NCBI36 |
NG_007572.1:g.7913_7914del , LRG_92:g.7913_7914del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.112-4_112-3del MANE Select | ENSP00000358548.4:n.112-4_112-3del | |
ENST00000369535.4:c.112-4_112-3del | ENSP00000358548.4:n.112-4_112-3del | |
NM_002524.4:c.112-4_112-3del | NP_002515.1:n.112-4_112-3del | |
NM_002524.5:c.112-4_112-3del MANE Select | NP_002515.1:n.112-4_112-3del |