HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41584053_41584061del , CM000679.2:g.41584053_41584061del | GRCh38 |
NC_000017.10:g.39740305_39740313del , CM000679.1:g.39740305_39740313del | GRCh37 |
NC_000017.9:g.36993831_36993839del | NCBI36 |
NG_008624.1:g.7835_7843del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.766-140_766-132del MANE Select | ENSP00000167586.6:n.766-140_766-132del | |
ENST00000167586.6:c.766-140_766-132del | ENSP00000167586.6:n.766-140_766-132del | |
ENST00000476662.1:n.216-140_216-132del | ||
NM_000526.4:c.766-140_766-132del | NP_000517.2:n.766-140_766-132del | |
NM_000526.5:c.766-140_766-132del MANE Select | NP_000517.3:n.766-140_766-132del |