HGVS | Genome Assembly |
---|---|
NC_000007.14:g.94409288_94409289delinsCT , CM000669.2:g.94409288_94409289delinsCT | GRCh38 |
NC_000007.13:g.94038600_94038601delinsCT , CM000669.1:g.94038600_94038601delinsCT | GRCh37 |
NC_000007.12:g.93876536_93876537delinsCT | NCBI36 |
NG_007405.1:g.19728_19729delinsCT , LRG_2:g.19728_19729delinsCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000297268.11:c.793-34_793-33delinsCT MANE Select | ENSP00000297268.6:n.793-34_793-33delinsCT... | |
ENST00000297268.10:c.793-34_793-33delinsCT | ENSP00000297268.6:n.793-34_793-33delinsCT... | |
ENST00000620463.1:c.787-34_787-33delinsCT | ENSP00000477719.1:n.787-34_787-33delinsCT... | |
NM_000089.3:c.793-34_793-33delinsCT , LRG_2t1:c.793-34_793-33delinsCT | NP_000080.2:n.793-34_793-33delinsCT | |
NM_000089.4:c.793-34_793-33delinsCT MANE Select | NP_000080.2:n.793-34_793-33delinsCT |