HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41584650_41584656del , CM000679.2:g.41584650_41584656del | GRCh38 |
NC_000017.10:g.39740902_39740908del , CM000679.1:g.39740902_39740908del | GRCh37 |
NC_000017.9:g.36994428_36994434del | NCBI36 |
NG_008624.1:g.7244_7250del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.609-239_609-233del MANE Select | ENSP00000167586.6:n.609-239_609-233del | |
ENST00000167586.6:c.609-239_609-233del | ENSP00000167586.6:n.609-239_609-233del | |
NM_000526.4:c.609-239_609-233del | NP_000517.2:n.609-239_609-233del | |
NM_000526.5:c.609-239_609-233del MANE Select | NP_000517.3:n.609-239_609-233del |