HGVS | Genome Assembly |
---|---|
NC_000012.12:g.91107261_91107296del , CM000674.2:g.91107261_91107296del | GRCh38 |
NC_000012.11:g.91501038_91501073del , CM000674.1:g.91501038_91501073del | GRCh37 |
NC_000012.10:g.90025169_90025204del | NCBI36 |
HGVS | Amino-acid change | |
---|---|---|
ENST00000266718.5:c.862+823_862+858del MANE Select | ENSP00000266718.4:n.862+823_862+858del | |
ENST00000266718.4:c.862+823_862+858del | ENSP00000266718.4:n.862+823_862+858del | |
ENST00000546642.1:n.612+823_612+858del | ||
ENST00000548071.1:n.255+823_255+858del | ||
NM_002345.3:c.862+823_862+858del | NP_002336.1:n.862+823_862+858del | |
NM_002345.4:c.862+823_862+858del MANE Select | NP_002336.1:n.862+823_862+858del |