HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41584061_41584074del , CM000679.2:g.41584061_41584074del | GRCh38 |
NC_000017.10:g.39740313_39740326del , CM000679.1:g.39740313_39740326del | GRCh37 |
NC_000017.9:g.36993839_36993852del | NCBI36 |
NG_008624.1:g.7823_7836del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.766-152_766-139del MANE Select | ENSP00000167586.6:n.766-152_766-139del | |
ENST00000167586.6:c.766-152_766-139del | ENSP00000167586.6:n.766-152_766-139del | |
ENST00000476662.1:n.216-152_216-139del | ||
NM_000526.4:c.766-152_766-139del | NP_000517.2:n.766-152_766-139del | |
NM_000526.5:c.766-152_766-139del MANE Select | NP_000517.3:n.766-152_766-139del |