HGVS | Genome Assembly |
---|---|
NC_000020.11:g.3084139_3084152dup , CM000682.2:g.3084139_3084152dup | GRCh38 |
NC_000020.10:g.3064785_3064798dup , CM000682.1:g.3064785_3064798dup | GRCh37 |
NC_000020.9:g.3012785_3012798dup | NCBI36 |
NG_008663.1:g.5579_5592dup , LRG_715:g.5579_5592dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000380293.3:c.120+409_120+422dup MANE Select | ENSP00000369647.3:n.120+409_120+422dup | |
NM_000490.4:c.120+409_120+422dup , LRG_715t1:c.120+409_120+422dup | NP_000481.2:n.120+409_120+422dup | |
XM_011529267.1:c.120+409_120+422dup | XP_011527569.1:n.120+409_120+422dup | |
XM_011529267.2:c.120+409_120+422dup | XP_011527569.1:n.120+409_120+422dup | |
NM_000490.5:c.120+409_120+422dup MANE Select | NP_000481.2:n.120+409_120+422dup |