HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21215676_21215678del , CM000674.2:g.21215676_21215678del | GRCh38 |
NC_000012.11:g.21368610_21368612del , CM000674.1:g.21368610_21368612del | GRCh37 |
NC_000012.10:g.21259877_21259879del | NCBI36 |
NG_011745.1:g.89483_89485del , LRG_1022:g.89483_89485del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256958.3:c.1498-1443_1498-1441del MANE Select | ENSP00000256958.2:n.1498-1443_1498-1441de... | |
ENST00000256958.2:c.1498-1443_1498-1441del | ENSP00000256958.2:n.1498-1443_1498-1441de... | |
NM_006446.4:c.1498-1443_1498-1441del , LRG_1022t1:c.1498-1443_1498-1441del | NP_006437.3:n.1498-1443_1498-1441del | |
NM_006446.5:c.1498-1443_1498-1441del MANE Select | NP_006437.3:n.1498-1443_1498-1441del |