HGVS | Genome Assembly |
---|---|
NC_000020.11:g.3084186_3084187delinsGC , CM000682.2:g.3084186_3084187delinsGC | GRCh38 |
NC_000020.10:g.3064832_3064833delinsGC , CM000682.1:g.3064832_3064833delinsGC | GRCh37 |
NC_000020.9:g.3012832_3012833delinsGC | NCBI36 |
NG_008663.1:g.5538_5539delinsGC , LRG_715:g.5538_5539delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000380293.3:c.120+368_120+369delinsGC MANE Select | ENSP00000369647.3:n.120+368_120+369delinsGC | |
NM_000490.4:c.120+368_120+369delinsGC , LRG_715t1:c.120+368_120+369delinsGC | NP_000481.2:n.120+368_120+369delinsGC | |
XM_011529267.1:c.120+368_120+369delinsGC | XP_011527569.1:n.120+368_120+369delinsGC | |
XM_011529267.2:c.120+368_120+369delinsGC | XP_011527569.1:n.120+368_120+369delinsGC | |
NM_000490.5:c.120+368_120+369delinsGC MANE Select | NP_000481.2:n.120+368_120+369delinsGC |