HGVS | Genome Assembly |
---|---|
NC_000014.9:g.23431395_23431411del , CM000676.2:g.23431395_23431411del | GRCh38 |
NC_000014.8:g.23900604_23900620del , CM000676.1:g.23900604_23900620del | GRCh37 |
NC_000014.7:g.22970444_22970460del | NCBI36 |
NG_007884.1:g.9251_9267del , LRG_384:g.9251_9267del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000355349.4:c.796+7_796+23del MANE Select | ENSP00000347507.3:n.796+7_796+23del | |
ENST00000355349.3:c.796+7_796+23del | ENSP00000347507.3:n.796+7_796+23del | |
NM_000257.3:c.796+7_796+23del | NP_000248.2:n.796+7_796+23del | |
XR_245686.3:n.902+7_902+23del | ||
XM_017021340.1:c.796+7_796+23del | XP_016876829.1:n.796+7_796+23del | |
NM_000257.4:c.796+7_796+23del MANE Select | NP_000248.2:n.796+7_796+23del |