HGVS | Genome Assembly |
---|---|
NC_000019.10:g.18787843_18787844dup , CM000681.2:g.18787843_18787844dup | GRCh38 |
NC_000019.9:g.18898652_18898653dup , CM000681.1:g.18898652_18898653dup | GRCh37 |
NC_000019.8:g.18759652_18759653dup | NCBI36 |
NG_007070.1:g.8464_8465dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222271.7:c.976-192_976-191dup MANE Select | ENSP00000222271.2:n.976-192_976-191dup | |
ENST00000222271.6:c.976-192_976-191dup | ENSP00000222271.2:n.976-192_976-191dup | |
ENST00000425807.1:c.817-192_817-191dup | ENSP00000403792.1:n.817-192_817-191dup | |
ENST00000542601.6:c.877-192_877-191dup | ENSP00000439156.2:n.877-192_877-191dup | |
NM_000095.2:c.976-192_976-191dup | NP_000086.2:n.976-192_976-191dup | |
NM_000095.3:c.976-192_976-191dup MANE Select | NP_000086.2:n.976-192_976-191dup |