HGVS | Genome Assembly |
---|---|
NC_000015.10:g.74752089del , CM000677.2:g.74752089del | GRCh38 |
NC_000015.9:g.75044430del , CM000677.1:g.75044430del | GRCh37 |
NC_000015.8:g.72831483del | NCBI36 |
NG_008431.1:g.34548del | |
NG_008431.2:g.34548del | |
NG_061543.1:g.8245del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000343932.5:c.1043-35del MANE Select | ENSP00000342007.4:n.1043-35del | |
ENST00000343932.4:c.1043-35del | ENSP00000342007.4:n.1043-35del | |
NM_000761.4:c.1043-35del | NP_000752.2:n.1043-35del | |
NM_000761.5:c.1043-35del MANE Select | NP_000752.2:n.1043-35del |