HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153740445_153740446insTTGGT , CM000685.2:g.153740445_153740446insTTGGT | GRCh38 |
NC_000023.10:g.153005899_153005900insTTGGT , CM000685.1:g.153005899_153005900insTTGGT | GRCh37 |
NC_000023.9:g.152659093_152659094insTTGGT | NCBI36 |
NG_009022.2:g.20578_20579insTTGGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218104.6:c.1635-129_1635-128insTTGGT MANE Select | ENSP00000218104.3:n.1635-129_1635-128insTTGGT | |
ENST00000218104.5:c.1635-129_1635-128insTTGGT | ENSP00000218104.3:n.1635-129_1635-128insTTGGT | |
ENST00000443684.2:n.638-129_638-128insTTGGT | ||
NM_000033.3:c.1635-129_1635-128insTTGGT | NP_000024.2:n.1635-129_1635-128insTTGGT | |
XR_938507.1:n.2107-129_2107-128insTTGGT | ||
XR_938507.2:n.2107-129_2107-128insTTGGT | ||
NM_000033.4:c.1635-129_1635-128insTTGGT MANE Select | NP_000024.2:n.1635-129_1635-128insTTGGT |