HGVS | Genome Assembly |
---|---|
NC_000021.9:g.44456801del , CM000683.2:g.44456801del | GRCh38 |
NC_000021.8:g.45876684del , CM000683.1:g.45876684del | GRCh37 |
NC_000021.7:g.44701112del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000291592.6:c.157del MANE Select | ENSP00000291592.4:p.Arg53GlyfsTer17 | |
ENST00000291592.5:c.157del | ENSP00000291592.4:p.Arg53GlyfsTer17 | |
NM_030891.4:c.157del | NP_112153.1:p.Arg53GlyfsTer17 | |
NM_030891.5:c.157del | NP_112153.1:p.Arg53GlyfsTer17 | |
NM_030891.6:c.157del MANE Select | NP_112153.1:p.Arg53GlyfsTer17 |