HGVS | Genome Assembly |
---|---|
NC_000017.11:g.29530399del , CM000679.2:g.29530399del | GRCh38 |
NC_000017.10:g.27857417del , CM000679.1:g.27857417del | GRCh37 |
NC_000017.9:g.24881543del | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261716.8:c.2149-8del MANE Select | ENSP00000261716.3:n.2149-8del | |
ENST00000261716.7:c.2149-8del | ENSP00000261716.3:n.2149-8del | |
ENST00000536202.1:c.1705-8del | ENSP00000438819.1:n.1705-8del | |
ENST00000578653.1:n.233-8del | ||
NM_020791.2:c.2149-8del | NP_065842.1:n.2149-8del | |
NM_025142.1:c.1705-8del | NP_079418.1:n.1705-8del | |
XM_011525060.1:c.2149-8del | XP_011523362.1:n.2149-8del | |
XM_011525060.2:c.2149-8del | XP_011523362.1:n.2149-8del | |
NM_020791.4:c.2149-8del MANE Select | NP_065842.1:n.2149-8del |