HGVS | Genome Assembly |
---|---|
NC_000005.10:g.136046528del , CM000667.2:g.136046528del | GRCh38 |
NC_000005.9:g.135382217del , CM000667.1:g.135382217del | GRCh37 |
NC_000005.8:g.135410116del | NCBI36 |
NG_012646.1:g.22634del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000442011.7:c.459+33del MANE Select | ENSP00000416330.2:n.459+33del | |
ENST00000442011.6:c.459+33del | ENSP00000416330.2:n.459+33del | |
ENST00000506699.5:n.557del | ||
ENST00000507018.5:c.409del | ||
ENST00000515433.1:n.784del | ||
NM_000358.2:c.459+33del | NP_000349.1:n.459+33del | |
NM_000358.3:c.459+33del MANE Select | NP_000349.1:n.459+33del |