HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153736080_153736096del , CM000685.2:g.153736080_153736096del | GRCh38 |
NC_000023.10:g.153001534_153001550del , CM000685.1:g.153001534_153001550del | GRCh37 |
NC_000023.9:g.152654728_152654744del | NCBI36 |
NG_009022.2:g.16213_16229del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218104.6:c.1082-32_1082-16del MANE Select | ENSP00000218104.3:n.1082-32_1082-16del | |
ENST00000218104.5:c.1082-32_1082-16del | ENSP00000218104.3:n.1082-32_1082-16del | |
ENST00000443684.2:n.85-32_85-16del | ||
NM_000033.3:c.1082-32_1082-16del | NP_000024.2:n.1082-32_1082-16del | |
XR_938507.1:n.1498-32_1498-16del | ||
XR_938507.2:n.1498-32_1498-16del | ||
NM_000033.4:c.1082-32_1082-16del MANE Select | NP_000024.2:n.1082-32_1082-16del |