HGVS | Genome Assembly |
---|---|
NC_000001.11:g.171652639del , CM000663.2:g.171652639del | GRCh38 |
NC_000001.10:g.171621779del , CM000663.1:g.171621779del | GRCh37 |
NC_000001.9:g.169888402del | NCBI36 |
NG_008859.1:g.4996del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000037502.11:c.-27del MANE Select | ENSP00000037502.5:n.-27del | |
ENST00000037502.10:c.-27del | ENSP00000037502.5:n.-27del | |
NM_000261.2:c.-27del MANE Select | NP_000252.1:n.-27del |