HGVS | Genome Assembly |
---|---|
NC_000020.11:g.3084254_3084258delinsTCTCC , CM000682.2:g.3084254_3084258delinsTCTCC | GRCh38 |
NC_000020.10:g.3064900_3064904delinsTCTCC , CM000682.1:g.3064900_3064904delinsTCTCC | GRCh37 |
NC_000020.9:g.3012900_3012904delinsTCTCC | NCBI36 |
NG_008663.1:g.5467_5471delinsGGAGA , LRG_715:g.5467_5471delinsGGAGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000380293.3:c.120+297_120+301delinsGGAGA MANE Select | ENSP00000369647.3:n.120+297_120+301delinsGGAGA | |
NM_000490.4:c.120+297_120+301delinsGGAGA , LRG_715t1:c.120+297_120+301delinsGGAGA | NP_000481.2:n.120+297_120+301delinsGGAGA | |
XM_011529267.1:c.120+297_120+301delinsGGAGA | XP_011527569.1:n.120+297_120+301delinsGGAGA | |
XM_011529267.2:c.120+297_120+301delinsGGAGA | XP_011527569.1:n.120+297_120+301delinsGGAGA | |
NM_000490.5:c.120+297_120+301delinsGGAGA MANE Select | NP_000481.2:n.120+297_120+301delinsGGAGA |