HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94041493_94041495del , CM000663.2:g.94041493_94041495del | GRCh38 |
NC_000001.10:g.94507049_94507051del , CM000663.1:g.94507049_94507051del | GRCh37 |
NC_000001.9:g.94279637_94279639del | NCBI36 |
NG_009073.1:g.84655_84657del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.3329-93_3329-91del MANE Select | ENSP00000359245.3:n.3329-93_3329-91del | |
ENST00000370225.3:c.3329-93_3329-91del | ENSP00000359245.3:n.3329-93_3329-91del | |
ENST00000536513.5:c.-64-1406_-64-1404del | ENSP00000439707.2:n.-64-1406_-64-1404del | |
NM_000350.2:c.3329-93_3329-91del | NP_000341.2:n.3329-93_3329-91del | |
NM_000350.3:c.3329-93_3329-91del MANE Select | NP_000341.2:n.3329-93_3329-91del |