HGVS | Genome Assembly |
---|---|
NC_000001.11:g.68429957_68429958del , CM000663.2:g.68429957_68429958del | GRCh38 |
NC_000001.10:g.68895640_68895641del , CM000663.1:g.68895640_68895641del | GRCh37 |
NC_000001.9:g.68668228_68668229del | NCBI36 |
NG_008472.1:g.25002_25003del | |
NG_008472.2:g.25002_25003del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262340.6:c.1451-31_1451-30del MANE Select | ENSP00000262340.5:n.1451-31_1451-30del | |
ENST00000262340.5:c.1451-31_1451-30del | ENSP00000262340.5:n.1451-31_1451-30del | |
NM_000329.2:c.1451-31_1451-30del | NP_000320.1:n.1451-31_1451-30del | |
XM_017002027.1:c.1175-31_1175-30del | XP_016857516.1:n.1175-31_1175-30del | |
NM_000329.3:c.1451-31_1451-30del MANE Select | NP_000320.1:n.1451-31_1451-30del |