HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114713732del , CM000663.2:g.114713732del | GRCh38 |
NC_000001.10:g.115256353del , CM000663.1:g.115256353del | GRCh37 |
NC_000001.9:g.115057876del | NCBI36 |
NG_007572.1:g.8164del , LRG_92:g.8164del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.290+69del MANE Select | ENSP00000358548.4:n.290+69del | |
ENST00000369535.4:c.290+69del | ENSP00000358548.4:n.290+69del | |
NM_002524.4:c.290+69del | NP_002515.1:n.290+69del | |
NM_002524.5:c.290+69del MANE Select | NP_002515.1:n.290+69del |