HGVS | Genome Assembly |
---|---|
NC_000001.11:g.68429988_68429989del , CM000663.2:g.68429988_68429989del | GRCh38 |
NC_000001.10:g.68895671_68895672del , CM000663.1:g.68895671_68895672del | GRCh37 |
NC_000001.9:g.68668259_68668260del | NCBI36 |
NG_008472.1:g.24971_24972del | |
NG_008472.2:g.24971_24972del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262340.6:c.1451-62_1451-61del MANE Select | ENSP00000262340.5:n.1451-62_1451-61del | |
ENST00000262340.5:c.1451-62_1451-61del | ENSP00000262340.5:n.1451-62_1451-61del | |
NM_000329.2:c.1451-62_1451-61del | NP_000320.1:n.1451-62_1451-61del | |
XM_017002027.1:c.1175-62_1175-61del | XP_016857516.1:n.1175-62_1175-61del | |
NM_000329.3:c.1451-62_1451-61del MANE Select | NP_000320.1:n.1451-62_1451-61del |