HGVS | Genome Assembly |
---|---|
NC_000020.11:g.10656351_10656354del , CM000682.2:g.10656351_10656354del | GRCh38 |
NC_000020.10:g.10636999_10637002del , CM000682.1:g.10636999_10637002del | GRCh37 |
NC_000020.9:g.10584999_10585002del | NCBI36 |
NG_007496.1:g.22695_22698del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000254958.10:c.755+46_755+49del MANE Select | ENSP00000254958.4:n.755+46_755+49del | |
ENST00000254958.9:c.755+46_755+49del | ENSP00000254958.4:n.755+46_755+49del | |
ENST00000423891.6:n.621+46_621+49del | ||
NM_000214.2:c.755+46_755+49del | NP_000205.1:n.755+46_755+49del | |
NM_000214.3:c.755+46_755+49del MANE Select | NP_000205.1:n.755+46_755+49del |