HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21215798_21215799del , CM000674.2:g.21215798_21215799del | GRCh38 |
NC_000012.11:g.21368732_21368733del , CM000674.1:g.21368732_21368733del | GRCh37 |
NC_000012.10:g.21259999_21260000del | NCBI36 |
NG_011745.1:g.89605_89606del , LRG_1022:g.89605_89606del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000256958.3:c.1498-1321_1498-1320del MANE Select | ENSP00000256958.2:n.1498-1321_1498-1320del | |
ENST00000256958.2:c.1498-1321_1498-1320del | ENSP00000256958.2:n.1498-1321_1498-1320del | |
NM_006446.4:c.1498-1321_1498-1320del , LRG_1022t1:c.1498-1321_1498-1320del | NP_006437.3:n.1498-1321_1498-1320del | |
NM_006446.5:c.1498-1321_1498-1320del MANE Select | NP_006437.3:n.1498-1321_1498-1320del |