HGVS | Genome Assembly |
---|---|
NC_000019.10:g.18787921_18787922del , CM000681.2:g.18787921_18787922del | GRCh38 |
NC_000019.9:g.18898730_18898731del , CM000681.1:g.18898730_18898731del | GRCh37 |
NC_000019.8:g.18759730_18759731del | NCBI36 |
NG_007070.1:g.8390_8391del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222271.7:c.976-266_976-265del MANE Select | ENSP00000222271.2:n.976-266_976-265del | |
ENST00000222271.6:c.976-266_976-265del | ENSP00000222271.2:n.976-266_976-265del | |
ENST00000425807.1:c.817-266_817-265del | ENSP00000403792.1:n.817-266_817-265del | |
ENST00000542601.6:c.877-266_877-265del | ENSP00000439156.2:n.877-266_877-265del | |
NM_000095.2:c.976-266_976-265del | NP_000086.2:n.976-266_976-265del | |
NM_000095.3:c.976-266_976-265del MANE Select | NP_000086.2:n.976-266_976-265del |