HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153742919_153742927del , CM000685.2:g.153742919_153742927del | GRCh38 |
NC_000023.10:g.153008373_153008381del , CM000685.1:g.153008373_153008381del | GRCh37 |
NC_000023.9:g.152661567_152661575del | NCBI36 |
NG_009022.2:g.23052_23060del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218104.6:c.1781-68_1781-60del MANE Select | ENSP00000218104.3:n.1781-68_1781-60del | |
ENST00000218104.5:c.1781-68_1781-60del | ENSP00000218104.3:n.1781-68_1781-60del | |
NM_000033.3:c.1781-68_1781-60del | NP_000024.2:n.1781-68_1781-60del | |
XR_938507.1:n.2253-68_2253-60del | ||
XR_938507.2:n.2253-68_2253-60del | ||
NM_000033.4:c.1781-68_1781-60del MANE Select | NP_000024.2:n.1781-68_1781-60del |