HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19961786_19961787delinsGC , CM000670.2:g.19961786_19961787delinsGC | GRCh38 |
NC_000008.10:g.19819297_19819298delinsGC , CM000670.1:g.19819297_19819298delinsGC | GRCh37 |
NC_000008.9:g.19863577_19863578delinsGC | NCBI36 |
NG_008855.1:g.27716_27717delinsGC | |
NG_008855.2:g.65070_65071delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650287.1:c.1323-329_1323-328delinsGC MANE Select | ENSP00000497642.1:n.1323-329_1323-328delinsGC | |
ENST00000650478.1:c.263-329_263-328delinsGC | ENSP00000497560.1:n.263-329_263-328delinsGC | |
ENST00000311322.8:c.1323-329_1323-328delinsGC | ENSP00000309757.6:n.1323-329_1323-328delinsGC | |
NM_000237.2:c.1323-329_1323-328delinsGC | NP_000228.1:n.1323-329_1323-328delinsGC | |
NM_000237.3:c.1323-329_1323-328delinsGC MANE Select | NP_000228.1:n.1323-329_1323-328delinsGC |