HGVS | Genome Assembly |
---|---|
NC_000008.11:g.19957518_19957521del , CM000670.2:g.19957518_19957521del | GRCh38 |
NC_000008.10:g.19815029_19815032del , CM000670.1:g.19815029_19815032del | GRCh37 |
NC_000008.9:g.19859309_19859312del | NCBI36 |
NG_008855.1:g.23448_23451del | |
NG_008855.2:g.60802_60805del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000650287.1:c.1018+1435_1018+1438del MANE Select | ENSP00000497642.1:n.1018+1435_1018+1438de... | |
ENST00000650478.1:c.79+1435_79+1438del | ENSP00000497560.1:n.79+1435_79+1438del | |
ENST00000311322.8:c.1018+1435_1018+1438del | ENSP00000309757.6:n.1018+1435_1018+1438de... | |
NM_000237.2:c.1018+1435_1018+1438del | NP_000228.1:n.1018+1435_1018+1438del | |
NM_000237.3:c.1018+1435_1018+1438del MANE Select | NP_000228.1:n.1018+1435_1018+1438del |