HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94046909del , CM000663.2:g.94046909del | GRCh38 |
NC_000001.10:g.94512465del , CM000663.1:g.94512465del | GRCh37 |
NC_000001.9:g.94285053del | NCBI36 |
NG_009073.1:g.79242del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000370225.4:c.2918+11del MANE Select | ENSP00000359245.3:n.2918+11del | |
ENST00000649773.1:c.2696+11del | ENSP00000496882.1:n.2696+11del | |
ENST00000370225.3:c.2918+11del | ENSP00000359245.3:n.2918+11del | |
ENST00000536513.5:c.-64-6819del | ENSP00000439707.2:n.-64-6819del | |
NM_000350.2:c.2918+11del | NP_000341.2:n.2918+11del | |
NM_000350.3:c.2918+11del MANE Select | NP_000341.2:n.2918+11del |