HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86643652del , CM000670.2:g.86643652del | GRCh38 |
NC_000008.10:g.87655880del , CM000670.1:g.87655880del | GRCh37 |
NC_000008.9:g.87724996del | NCBI36 |
NG_016980.1:g.105026del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320005.6:c.1178+101del MANE Select | ENSP00000316605.5:n.1178+101del | |
ENST00000681546.1:n.998+101del | ||
ENST00000681746.1:c.1178+101del | ENSP00000505959.1:n.1178+101del | |
ENST00000320005.5:c.1178+101del | ENSP00000316605.5:n.1178+101del | |
NM_019098.4:c.1178+101del | NP_061971.3:n.1178+101del | |
XM_011517138.1:c.764+101del | XP_011515440.1:n.764+101del | |
XM_011517138.2:c.764+101del | XP_011515440.1:n.764+101del | |
NM_019098.5:c.1178+101del MANE Select | NP_061971.3:n.1178+101del |