HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41583156del , CM000679.2:g.41583156del | GRCh38 |
NC_000017.10:g.39739408del , CM000679.1:g.39739408del | GRCh37 |
NC_000017.9:g.36992934del | NCBI36 |
NG_008624.1:g.8743del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.1275-13del MANE Select | ENSP00000167586.6:n.1275-13del | |
ENST00000167586.6:c.1275-13del | ENSP00000167586.6:n.1275-13del | |
ENST00000441550.2:n.222-13del | ||
NM_000526.4:c.1275-13del | NP_000517.2:n.1275-13del | |
NM_000526.5:c.1275-13del MANE Select | NP_000517.3:n.1275-13del |