HGVS | Genome Assembly |
---|---|
NC_000011.10:g.2445168del , CM000673.2:g.2445168del | GRCh38 |
NC_000011.9:g.2466398del , CM000673.1:g.2466398del | GRCh37 |
NC_000011.8:g.2422974del | NCBI36 |
NG_008935.1:g.5178del , LRG_287:g.5178del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000496887.7:c.24-215del | ENSP00000434560.2:n.24-215del | |
ENST00000646564.2:c.70del | ENSP00000495806.2:p.Arg24GlyfsTer? | |
ENST00000155840.12:c.70del MANE Select | ENSP00000155840.2:p.Arg24GlyfsTer? | |
ENST00000155840.9:c.70del | ENSP00000155840.2:p.Arg24GlyfsTer? | |
ENST00000496887.6:c.24-215del | ENSP00000434560.1:n.24-215del | |
NM_000218.2:c.70del , LRG_287t1:c.70del | NP_000209.2:p.Arg24GlyfsTer? | |
NM_000218.3:c.70del MANE Select | NP_000209.2:p.Arg24GlyfsTer? |