HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153736075_153736076insA , CM000685.2:g.153736075_153736076insA | GRCh38 |
NC_000023.10:g.153001529_153001530insA , CM000685.1:g.153001529_153001530insA | GRCh37 |
NC_000023.9:g.152654723_152654724insA | NCBI36 |
NG_009022.2:g.16208_16209insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218104.6:c.1082-37_1082-36insA MANE Select | ENSP00000218104.3:n.1082-37_1082-36insA | |
ENST00000218104.5:c.1082-37_1082-36insA | ENSP00000218104.3:n.1082-37_1082-36insA | |
ENST00000443684.2:n.85-37_85-36insA | ||
NM_000033.3:c.1082-37_1082-36insA | NP_000024.2:n.1082-37_1082-36insA | |
XR_938507.1:n.1498-37_1498-36insA | ||
XR_938507.2:n.1498-37_1498-36insA | ||
NM_000033.4:c.1082-37_1082-36insA MANE Select | NP_000024.2:n.1082-37_1082-36insA |