HGVS | Genome Assembly |
---|---|
NC_000002.12:g.29070689_29070691del , CM000664.2:g.29070689_29070691del | GRCh38 |
NC_000002.11:g.29293555_29293557del , CM000664.1:g.29293555_29293557del | GRCh37 |
NC_000002.10:g.29147059_29147061del | NCBI36 |
NG_021427.1:g.8575_8577del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331664.6:c.3575_3577del MANE Select | ENSP00000332809.4:p.Arg1192del | |
ENST00000331664.5:c.3575_3577del | ENSP00000332809.4:p.Arg1192del | |
NM_001029883.2:c.3575_3577del | NP_001025054.1:p.Arg1192del | |
XM_011532826.1:c.3575_3577del | XP_011531128.1:p.Arg1192del | |
XR_939901.1:n.185+1522_185+1524del | ||
XR_939902.1:n.173+1534_173+1536del | ||
NM_001029883.3:c.3575_3577del MANE Select | NP_001025054.1:p.Arg1192del |