HGVS | Genome Assembly |
---|---|
NC_000022.11:g.27750748del , CM000684.2:g.27750748del | GRCh38 |
NC_000022.10:g.28146736del , CM000684.1:g.28146736del | GRCh37 |
NC_000022.9:g.26476736del | NCBI36 |
NG_023258.1:g.55752del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000703102.1:n.656del | ||
ENST00000302326.5:c.*168del MANE Select | ENSP00000304956.4:n.*168del | |
ENST00000302326.4:c.*168del | ENSP00000304956.4:n.*168del | |
ENST00000424656.1:c.455+29del | ||
ENST00000497225.1:n.487del | ||
NM_002430.2:c.*168del | NP_002421.3:n.*168del | |
NM_002430.3:c.*168del MANE Select | NP_002421.3:n.*168del |