HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153736069_153736083del , CM000685.2:g.153736069_153736083del | GRCh38 |
NC_000023.10:g.153001523_153001537del , CM000685.1:g.153001523_153001537del | GRCh37 |
NC_000023.9:g.152654717_152654731del | NCBI36 |
NG_009022.2:g.16202_16216del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218104.6:c.1082-43_1082-29del MANE Select | ENSP00000218104.3:n.1082-43_1082-29del | |
ENST00000218104.5:c.1082-43_1082-29del | ENSP00000218104.3:n.1082-43_1082-29del | |
ENST00000443684.2:n.85-43_85-29del | ||
NM_000033.3:c.1082-43_1082-29del | NP_000024.2:n.1082-43_1082-29del | |
XR_938507.1:n.1498-43_1498-29del | ||
XR_938507.2:n.1498-43_1498-29del | ||
NM_000033.4:c.1082-43_1082-29del MANE Select | NP_000024.2:n.1082-43_1082-29del |