HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21216101del , CM000674.2:g.21216101del | GRCh38 |
NC_000012.11:g.21369035del , CM000674.1:g.21369035del | GRCh37 |
NC_000012.10:g.21260302del | NCBI36 |
NG_011745.1:g.89908del , LRG_1022:g.89908del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256958.3:c.1498-1018del MANE Select | ENSP00000256958.2:n.1498-1018del | |
ENST00000256958.2:c.1498-1018del | ENSP00000256958.2:n.1498-1018del | |
NM_006446.4:c.1498-1018del , LRG_1022t1:c.1498-1018del | NP_006437.3:n.1498-1018del | |
NM_006446.5:c.1498-1018del MANE Select | NP_006437.3:n.1498-1018del |