HGVS | Genome Assembly |
---|---|
NC_000008.11:g.86643610del , CM000670.2:g.86643610del | GRCh38 |
NC_000008.10:g.87655838del , CM000670.1:g.87655838del | GRCh37 |
NC_000008.9:g.87724954del | NCBI36 |
NG_016980.1:g.105066del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000320005.6:c.1178+141del MANE Select | ENSP00000316605.5:n.1178+141del | |
ENST00000681546.1:n.998+141del | ||
ENST00000681746.1:c.1178+141del | ENSP00000505959.1:n.1178+141del | |
ENST00000320005.5:c.1178+141del | ENSP00000316605.5:n.1178+141del | |
NM_019098.4:c.1178+141del | NP_061971.3:n.1178+141del | |
XM_011517138.1:c.764+141del | XP_011515440.1:n.764+141del | |
XM_011517138.2:c.764+141del | XP_011515440.1:n.764+141del | |
NM_019098.5:c.1178+141del MANE Select | NP_061971.3:n.1178+141del |