HGVS | Genome Assembly |
---|---|
NC_000019.10:g.7525202_7525205del , CM000681.2:g.7525202_7525205del | GRCh38 |
NC_000019.9:g.7590088_7590091del , CM000681.1:g.7590088_7590091del | GRCh37 |
NC_000019.8:g.7496088_7496091del | NCBI36 |
NG_015806.1:g.7593_7596del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264079.11:c.237+36_237+39del MANE Select | ENSP00000264079.5:n.237+36_237+39del | |
ENST00000264079.10:c.237+36_237+39del | ENSP00000264079.5:n.237+36_237+39del | |
ENST00000394321.9:n.317+36_317+39del | ||
ENST00000596390.1:n.389_392del | ||
ENST00000601003.1:c.237+36_237+39del | ENSP00000469074.1:n.237+36_237+39del | |
NM_020533.2:c.237+36_237+39del | NP_065394.1:n.237+36_237+39del | |
NM_020533.3:c.237+36_237+39del MANE Select | NP_065394.1:n.237+36_237+39del |