HGVS | Genome Assembly |
---|---|
NC_000012.12:g.76346170_76346171del , CM000674.2:g.76346170_76346171del | GRCh38 |
NC_000012.11:g.76739950_76739951del , CM000674.1:g.76739950_76739951del | GRCh37 |
NC_000012.10:g.75264081_75264082del | NCBI36 |
NG_016357.1:g.7272_7273del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000650064.2:c.1814_1815del MANE Select | ENSP00000497413.1:p.Asn605IlefsTer2 | |
ENST00000393262.3:c.1814_1815del | ENSP00000376946.3:p.Asn605IlefsTer2 | |
NM_024685.3:c.1814_1815del | NP_078961.3:p.Asn605IlefsTer2 | |
NM_024685.4:c.1814_1815del MANE Select | NP_078961.3:p.Asn605IlefsTer2 |