HGVS | Genome Assembly |
---|---|
NC_000015.10:g.74749715_74749716delinsCT , CM000677.2:g.74749715_74749716delinsCT | GRCh38 |
NC_000015.9:g.75042056_75042057delinsCT , CM000677.1:g.75042056_75042057delinsCT | GRCh37 |
NC_000015.8:g.72829109_72829110delinsCT | NCBI36 |
NG_008431.1:g.32174_32175delinsCT | |
NG_008431.2:g.32174_32175delinsCT | |
NG_061543.1:g.5871_5872delinsCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000343932.5:c.-9-15_-9-14delinsCT MANE Select | ENSP00000342007.4:n.-9-15_-9-14delinsCT | |
ENST00000343932.4:c.-9-15_-9-14delinsCT | ENSP00000342007.4:n.-9-15_-9-14delinsCT | |
NM_000761.4:c.-9-15_-9-14delinsCT | NP_000752.2:n.-9-15_-9-14delinsCT | |
NM_000761.5:c.-9-15_-9-14delinsCT MANE Select | NP_000752.2:n.-9-15_-9-14delinsCT |