HGVS | Genome Assembly |
---|---|
NC_000007.14:g.98391981_98391990del , CM000669.2:g.98391981_98391990del | GRCh38 |
NC_000007.13:g.98021293_98021302del , CM000669.1:g.98021293_98021302del | GRCh37 |
NC_000007.12:g.97859229_97859238del | NCBI36 |
NG_013090.1:g.14128_14137del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000005260.9:c.51+8814_51+8823del MANE Select | ENSP00000005260.8:n.51+8814_51+8823del | |
ENST00000005260.8:c.51+8814_51+8823del | ENSP00000005260.8:n.51+8814_51+8823del | |
ENST00000462558.5:n.267+8814_267+8823del | ||
ENST00000479789.1:n.357+7993_357+8002del | ||
NM_018842.4:c.51+8814_51+8823del | NP_061330.2:n.51+8814_51+8823del | |
NM_018842.5:c.51+8814_51+8823del MANE Select | NP_061330.2:n.51+8814_51+8823del |