HGVS | Genome Assembly |
---|---|
NC_000011.10:g.62909323_62909334del , CM000673.2:g.62909323_62909334del | GRCh38 |
NC_000011.9:g.62676795_62676806del , CM000673.1:g.62676795_62676806del | GRCh37 |
NC_000011.8:g.62433371_62433382del | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000306960.4:c.*384_*395del MANE Select | ENSP00000306490.3:n.*384_*395del | |
ENST00000306960.3:c.*384_*395del | ENSP00000306490.3:n.*384_*395del | |
NM_000738.2:c.*384_*395del | NP_000729.2:n.*384_*395del | |
XM_011544742.1:c.*384_*395del | XP_011543044.1:n.*384_*395del | |
XM_011544742.2:c.*384_*395del | XP_011543044.1:n.*384_*395del | |
NM_000738.3:c.*384_*395del MANE Select | NP_000729.2:n.*384_*395del |