HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171652665_171652666insACT , CM000663.2:g.171652665_171652666insACT | GRCh38 |
NC_000001.10:g.171621805_171621806insACT , CM000663.1:g.171621805_171621806insACT | GRCh37 |
NC_000001.9:g.169888428_169888429insACT | NCBI36 |
NG_008859.1:g.4968_4969insAGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.-55_-54insAGT MANE Select | ENSP00000037502.5:n.-55_-54insAGT | |
ENST00000037502.10:c.-55_-54insAGT | ENSP00000037502.5:n.-55_-54insAGT | |
NM_000261.2:c.-55_-54insAGT MANE Select | NP_000252.1:n.-55_-54insAGT |