HGVS | Genome Assembly |
---|---|
NC_000002.12:g.184915107_184915108insTCTGTAA , CM000664.2:g.184915107_184915108insTCTGTAA | GRCh38 |
NC_000002.11:g.185779834_185779835insTCTGTAA , CM000664.1:g.185779834_185779835insTCTGTAA | GRCh37 |
NC_000002.10:g.185488079_185488080insTCTGTAA | NCBI36 |
NG_046950.1:g.321742_321743insTCTGTAA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000302277.7:c.256-18496_256-18495insTCTGTAA MANE Select | ENSP00000303252.6:n.256-18496_256-18495insTCTGTAA | |
ENST00000302277.6:c.256-18496_256-18495insTCTGTAA | ENSP00000303252.6:n.256-18496_256-18495insTCTGTAA | |
ENST00000613975.1:c.1-18496_1-18495insTCTGTAA | ENSP00000483032.1:n.1-18496_1-18495insTCTGTAA | |
NM_194250.1:c.256-18496_256-18495insTCTGTAA | NP_919226.1:n.256-18496_256-18495insTCTGTAA | |
NM_194250.2:c.256-18496_256-18495insTCTGTAA MANE Select | NP_919226.1:n.256-18496_256-18495insTCTGTAA |