HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91107297_91107326del , CM000674.2:g.91107297_91107326del | GRCh38 |
NC_000012.11:g.91501074_91501103del , CM000674.1:g.91501074_91501103del | GRCh37 |
NC_000012.10:g.90025205_90025234del | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000266718.5:c.862+793_862+822del MANE Select | ENSP00000266718.4:n.862+793_862+822del | |
ENST00000266718.4:c.862+793_862+822del | ENSP00000266718.4:n.862+793_862+822del | |
ENST00000546642.1:n.612+793_612+822del | ||
ENST00000548071.1:n.255+793_255+822del | ||
NM_002345.3:c.862+793_862+822del | NP_002336.1:n.862+793_862+822del | |
NM_002345.4:c.862+793_862+822del MANE Select | NP_002336.1:n.862+793_862+822del |