HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41584057_41584069del , CM000679.2:g.41584057_41584069del | GRCh38 |
NC_000017.10:g.39740309_39740321del , CM000679.1:g.39740309_39740321del | GRCh37 |
NC_000017.9:g.36993835_36993847del | NCBI36 |
NG_008624.1:g.7827_7839del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.766-148_766-136del MANE Select | ENSP00000167586.6:n.766-148_766-136del | |
ENST00000167586.6:c.766-148_766-136del | ENSP00000167586.6:n.766-148_766-136del | |
ENST00000476662.1:n.216-148_216-136del | ||
NM_000526.4:c.766-148_766-136del | NP_000517.2:n.766-148_766-136del | |
NM_000526.5:c.766-148_766-136del MANE Select | NP_000517.3:n.766-148_766-136del |