HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21215639del , CM000674.2:g.21215639del | GRCh38 |
NC_000012.11:g.21368573del , CM000674.1:g.21368573del | GRCh37 |
NC_000012.10:g.21259840del | NCBI36 |
NG_011745.1:g.89446del , LRG_1022:g.89446del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256958.3:c.1498-1480del MANE Select | ENSP00000256958.2:n.1498-1480del | |
ENST00000256958.2:c.1498-1480del | ENSP00000256958.2:n.1498-1480del | |
NM_006446.4:c.1498-1480del , LRG_1022t1:c.1498-1480del | NP_006437.3:n.1498-1480del | |
NM_006446.5:c.1498-1480del MANE Select | NP_006437.3:n.1498-1480del |