HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171652664_171652665insT , CM000663.2:g.171652664_171652665insT | GRCh38 |
NC_000001.10:g.171621804_171621805insT , CM000663.1:g.171621804_171621805insT | GRCh37 |
NC_000001.9:g.169888427_169888428insT | NCBI36 |
NG_008859.1:g.4969_4970insA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.-54_-53insA MANE Select | ENSP00000037502.5:n.-54_-53insA | |
ENST00000037502.10:c.-54_-53insA | ENSP00000037502.5:n.-54_-53insA | |
NM_000261.2:c.-54_-53insA MANE Select | NP_000252.1:n.-54_-53insA |