HGVS | Genome Assembly |
---|---|
NC_000004.12:g.4862663_4862664delinsCT , CM000666.2:g.4862663_4862664delinsCT | GRCh38 |
NC_000004.11:g.4864390_4864391delinsCT , CM000666.1:g.4864390_4864391delinsCT | GRCh37 |
NC_000004.10:g.4915291_4915292delinsCT | NCBI36 |
NG_008121.1:g.7999_8000delinsCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382723.5:c.470-38_470-37delinsCT MANE Select | ENSP00000372170.4:n.470-38_470-37delinsCT | |
ENST00000382723.4:c.470-38_470-37delinsCT | ENSP00000372170.4:n.470-38_470-37delinsCT | |
ENST00000468421.1:n.182-38_182-37delinsCT | ||
NM_002448.3:c.470-38_470-37delinsCT MANE Select | NP_002439.2:n.470-38_470-37delinsCT |