HGVS | Genome Assembly |
---|---|
NC_000011.10:g.640123_640170del , CM000673.2:g.640123_640170del | GRCh38 |
NC_000011.9:g.640123_640170del , CM000673.1:g.640123_640170del | GRCh37 |
NC_000011.8:g.630123_630170del | NCBI36 |
NG_021241.1:g.7819_7866del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000176183.6:c.874_921del MANE Select | ENSP00000176183.5:p.Pro292_Gly307del | |
ENST00000176183.5:c.874_921del | ENSP00000176183.5:p.Pro292_Gly307del | |
NM_000797.3:c.874_921del | NP_000788.2:p.Pro292_Gly307del | |
NM_000797.4:c.874_921del MANE Select | NP_000788.2:p.Pro292_Gly307del |