HGVS | Genome Assembly |
---|---|
NC_000012.12:g.21215611_21215620dup , CM000674.2:g.21215611_21215620dup | GRCh38 |
NC_000012.11:g.21368545_21368554dup , CM000674.1:g.21368545_21368554dup | GRCh37 |
NC_000012.10:g.21259812_21259821dup | NCBI36 |
NG_011745.1:g.89418_89427dup , LRG_1022:g.89418_89427dup |
HGVS | Amino-acid change | |
---|---|---|
ENST00000256958.3:c.1498-1508_1498-1499dup MANE Select | ENSP00000256958.2:n.1498-1508_1498-1499du... | |
ENST00000256958.2:c.1498-1508_1498-1499dup | ENSP00000256958.2:n.1498-1508_1498-1499du... | |
NM_006446.4:c.1498-1508_1498-1499dup , LRG_1022t1:c.1498-1508_1498-1499dup | NP_006437.3:n.1498-1508_1498-1499dup | |
NM_006446.5:c.1498-1508_1498-1499dup MANE Select | NP_006437.3:n.1498-1508_1498-1499dup |