HGVS | Genome Assembly |
---|---|
NC_000022.11:g.27750773_27750776del , CM000684.2:g.27750773_27750776del | GRCh38 |
NC_000022.10:g.28146761_28146764del , CM000684.1:g.28146761_28146764del | GRCh37 |
NC_000022.9:g.26476761_26476764del | NCBI36 |
NG_023258.1:g.55726_55729del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000703102.1:n.630_633del | ||
ENST00000302326.5:c.*142_*145del MANE Select | ENSP00000304956.4:n.*142_*145del | |
ENST00000302326.4:c.*142_*145del | ENSP00000304956.4:n.*142_*145del | |
ENST00000424656.1:c.455+3_455+6del | ||
ENST00000497225.1:n.461_464del | ||
NM_002430.2:c.*142_*145del | NP_002421.3:n.*142_*145del | |
NM_002430.3:c.*142_*145del MANE Select | NP_002421.3:n.*142_*145del |