HGVS | Genome Assembly |
---|---|
NC_000001.11:g.68444567del , CM000663.2:g.68444567del | GRCh38 |
NC_000001.10:g.68910250del , CM000663.1:g.68910250del | GRCh37 |
NC_000001.9:g.68682838del | NCBI36 |
NG_008472.1:g.10395del | |
NG_008472.2:g.10395del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262340.6:c.461del MANE Select | ENSP00000262340.5:p.Lys154ArgfsTer? | |
ENST00000262340.5:c.461del | ENSP00000262340.5:p.Lys154ArgfsTer? | |
NM_000329.2:c.461del | NP_000320.1:p.Lys154ArgfsTer? | |
XM_017002027.1:c.185del | XP_016857516.1:p.Lys62ArgfsTer? | |
NM_000329.3:c.461del MANE Select | NP_000320.1:p.Lys154ArgfsTer? |