HGVS | Genome Assembly |
---|---|
NC_000019.10:g.18787678_18787680dup , CM000681.2:g.18787678_18787680dup | GRCh38 |
NC_000019.9:g.18898487_18898489dup , CM000681.1:g.18898487_18898489dup | GRCh37 |
NC_000019.8:g.18759487_18759489dup | NCBI36 |
NG_007070.1:g.8626_8628dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222271.7:c.976-30_976-28dup MANE Select | ENSP00000222271.2:n.976-30_976-28dup | |
ENST00000222271.6:c.976-30_976-28dup | ENSP00000222271.2:n.976-30_976-28dup | |
ENST00000425807.1:c.817-30_817-28dup | ENSP00000403792.1:n.817-30_817-28dup | |
ENST00000542601.6:c.877-30_877-28dup | ENSP00000439156.2:n.877-30_877-28dup | |
NM_000095.2:c.976-30_976-28dup | NP_000086.2:n.976-30_976-28dup | |
NM_000095.3:c.976-30_976-28dup MANE Select | NP_000086.2:n.976-30_976-28dup |