HGVS | Genome Assembly |
---|---|
NC_000006.12:g.38683096_38683104del , CM000668.2:g.38683096_38683104del | GRCh38 |
NC_000006.11:g.38650872_38650880del , CM000668.1:g.38650872_38650880del | GRCh37 |
NC_000006.10:g.38758850_38758858del | NCBI36 |
NG_012074.1:g.25075_25083del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373365.5:c.309-227_309-219del MANE Select | ENSP00000362463.3:n.309-227_309-219del | |
ENST00000373365.4:c.309-227_309-219del | ENSP00000362463.3:n.309-227_309-219del | |
ENST00000470973.1:n.114_122del | ||
NM_006708.2:c.309-227_309-219del | NP_006699.2:n.309-227_309-219del | |
NM_006708.3:c.309-227_309-219del MANE Select | NP_006699.2:n.309-227_309-219del |