HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17401108_17401111del , CM000663.2:g.17401108_17401111del | GRCh38 |
NC_000001.10:g.17727604_17727607del , CM000663.1:g.17727604_17727607del | GRCh37 |
NC_000001.9:g.17600191_17600194del | NCBI36 |
NG_032943.1:g.33863_33866del | |
NG_032943.2:g.33863_33866del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000619609.1:c.1852-97_1852-94del MANE Select | ENSP00000483125.1:n.1852-97_1852-94del | |
NM_207421.4:c.1852-97_1852-94del MANE Select | NP_997304.3:n.1852-97_1852-94del |