HGVS | Genome Assembly |
---|---|
NC_000005.10:g.177993062del , CM000667.2:g.177993062del | GRCh38 |
NC_000005.9:g.177420063del , CM000667.1:g.177420063del | GRCh37 |
NC_000005.8:g.177352669del | NCBI36 |
NG_015889.1:g.8182del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000308304.2:c.343-14del MANE Select | ENSP00000311290.2:n.343-14del | |
NM_006261.4:c.343-14del | NP_006252.3:n.343-14del | |
NM_006261.5:c.343-14del MANE Select | NP_006252.4:n.343-14del |