HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153736033_153736041del , CM000685.2:g.153736033_153736041del | GRCh38 |
NC_000023.10:g.153001487_153001495del , CM000685.1:g.153001487_153001495del | GRCh37 |
NC_000023.9:g.152654681_152654689del | NCBI36 |
NG_009022.2:g.16166_16174del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218104.6:c.1082-79_1082-71del MANE Select | ENSP00000218104.3:n.1082-79_1082-71del | |
ENST00000218104.5:c.1082-79_1082-71del | ENSP00000218104.3:n.1082-79_1082-71del | |
ENST00000443684.2:n.85-79_85-71del | ||
NM_000033.3:c.1082-79_1082-71del | NP_000024.2:n.1082-79_1082-71del | |
XR_938507.1:n.1498-79_1498-71del | ||
XR_938507.2:n.1498-79_1498-71del | ||
NM_000033.4:c.1082-79_1082-71del MANE Select | NP_000024.2:n.1082-79_1082-71del |