HGVS | Genome Assembly |
---|---|
NC_000020.11:g.3082887_3082893del , CM000682.2:g.3082887_3082893del | GRCh38 |
NC_000020.10:g.3063533_3063539del , CM000682.1:g.3063533_3063539del | GRCh37 |
NC_000020.9:g.3011533_3011539del | NCBI36 |
NG_008663.1:g.6832_6838del , LRG_715:g.6832_6838del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000380293.3:c.322+84_323-85del MANE Select | ENSP00000369647.3:n.322+84_323-85del | |
NM_000490.4:c.322+84_323-85del , LRG_715t1:c.322+84_323-85del | NP_000481.2:n.322+84_323-85del | |
XM_011529267.1:c.322+84_323-85del | XP_011527569.1:n.322+84_323-85del | |
XM_011529267.2:c.322+84_323-85del | XP_011527569.1:n.322+84_323-85del | |
NM_000490.5:c.322+84_323-85del MANE Select | NP_000481.2:n.322+84_323-85del |