HGVS | Genome Assembly |
---|---|
NC_000017.11:g.72123473_72123476del , CM000679.2:g.72123473_72123476del | GRCh38 |
NC_000017.10:g.70119614_70119617del , CM000679.1:g.70119614_70119617del | GRCh37 |
NC_000017.9:g.67631209_67631212del | NCBI36 |
NG_012490.1:g.7454_7457del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000245479.3:c.686-70_686-67del MANE Select | ENSP00000245479.2:n.686-70_686-67del | |
ENST00000245479.2:c.686-70_686-67del | ENSP00000245479.2:n.686-70_686-67del | |
NM_000346.3:c.686-70_686-67del | NP_000337.1:n.686-70_686-67del | |
NM_000346.4:c.686-70_686-67del MANE Select | NP_000337.1:n.686-70_686-67del |