HGVS | Genome Assembly |
---|---|
NC_000024.10:g.20583232del , CM000686.2:g.20583232del | GRCh38 |
NC_000024.9:g.22745118del , CM000686.1:g.22745118del | GRCh37 |
NC_000024.8:g.21154506del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361365.7:c.204+539del MANE Select | ENSP00000354722.2:n.204+539del | |
ENST00000361365.6:c.204+539del | ENSP00000354722.2:n.204+539del | |
ENST00000382772.3:c.204+539del | ENSP00000372222.3:n.204+539del | |
ENST00000465253.1:n.298+539del | ||
NM_001278612.1:c.204+539del | NP_001265541.1:n.204+539del | |
NM_004681.3:c.204+539del | NP_004672.2:n.204+539del | |
NM_004681.4:c.204+539del MANE Select | NP_004672.2:n.204+539del | |
NM_001278612.2:c.204+539del | NP_001265541.1:n.204+539del |