HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153736062_153736066del , CM000685.2:g.153736062_153736066del | GRCh38 |
NC_000023.10:g.153001516_153001520del , CM000685.1:g.153001516_153001520del | GRCh37 |
NC_000023.9:g.152654710_152654714del | NCBI36 |
NG_009022.2:g.16195_16199del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218104.6:c.1082-50_1082-46del MANE Select | ENSP00000218104.3:n.1082-50_1082-46del | |
ENST00000218104.5:c.1082-50_1082-46del | ENSP00000218104.3:n.1082-50_1082-46del | |
ENST00000443684.2:n.85-50_85-46del | ||
NM_000033.3:c.1082-50_1082-46del | NP_000024.2:n.1082-50_1082-46del | |
XR_938507.1:n.1498-50_1498-46del | ||
XR_938507.2:n.1498-50_1498-46del | ||
NM_000033.4:c.1082-50_1082-46del MANE Select | NP_000024.2:n.1082-50_1082-46del |