HGVS | Genome Assembly |
---|---|
NC_000001.11:g.186174431del , CM000663.2:g.186174431del | GRCh38 |
NC_000001.10:g.186143563del , CM000663.1:g.186143563del | GRCh37 |
NC_000001.9:g.184410186del | NCBI36 |
NG_011841.1:g.444881del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000271588.9:c.15815-83del MANE Select | ENSP00000271588.4:n.15815-83del | |
ENST00000271588.8:c.15815-83del | ENSP00000271588.4:n.15815-83del | |
ENST00000414277.1:c.191-83del | ENSP00000406205.1:n.191-83del | |
NM_031935.2:c.15815-83del | NP_114141.2:n.15815-83del | |
XM_011510037.1:c.15530-83del | XP_011508339.1:n.15530-83del | |
XM_011510038.1:c.15815-83del | XP_011508340.1:n.15815-83del | |
XM_011510038.3:c.15815-83del | XP_011508340.1:n.15815-83del | |
XM_017002437.1:c.13838-83del | XP_016857926.1:n.13838-83del | |
NM_031935.3:c.15815-83del MANE Select | NP_114141.2:n.15815-83del |