HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94051753_94051757del , CM000663.2:g.94051753_94051757del | GRCh38 |
NC_000001.10:g.94517309_94517313del , CM000663.1:g.94517309_94517313del | GRCh37 |
NC_000001.9:g.94289897_94289901del | NCBI36 |
NG_009073.1:g.74397_74401del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370225.4:c.2588-55_2588-51del MANE Select | ENSP00000359245.3:n.2588-55_2588-51del | |
ENST00000649773.1:c.2366-55_2366-51del | ENSP00000496882.1:n.2366-55_2366-51del | |
ENST00000370225.3:c.2588-55_2588-51del | ENSP00000359245.3:n.2588-55_2588-51del | |
ENST00000536513.5:c.-65+11421_-65+11425del | ENSP00000439707.2:n.-65+11421_-65+11425del | |
NM_000350.2:c.2588-55_2588-51del | NP_000341.2:n.2588-55_2588-51del | |
NM_000350.3:c.2588-55_2588-51del MANE Select | NP_000341.2:n.2588-55_2588-51del |