HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41584035_41584039del , CM000679.2:g.41584035_41584039del | GRCh38 |
NC_000017.10:g.39740287_39740291del , CM000679.1:g.39740287_39740291del | GRCh37 |
NC_000017.9:g.36993813_36993817del | NCBI36 |
NG_008624.1:g.7857_7861del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.766-118_766-114del MANE Select | ENSP00000167586.6:n.766-118_766-114del | |
ENST00000167586.6:c.766-118_766-114del | ENSP00000167586.6:n.766-118_766-114del | |
ENST00000476662.1:n.216-118_216-114del | ||
NM_000526.4:c.766-118_766-114del | NP_000517.2:n.766-118_766-114del | |
NM_000526.5:c.766-118_766-114del MANE Select | NP_000517.3:n.766-118_766-114del |