HGVS | Genome Assembly |
---|---|
NC_000006.12:g.29946099_29946101del , CM000668.2:g.29946099_29946101del | GRCh38 |
NC_000006.11:g.29913876_29913878del , CM000668.1:g.29913876_29913878del | GRCh37 |
NC_000006.10:g.30021855_30021857del | NCBI36 |
NG_029217.2:g.8635_8637del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000706901.1:c.*644_*646del | ENSP00000516612.1:n.*644_*646del | |
ENST00000706902.1:c.1093+818_1093+820del | ENSP00000516613.1:n.1093+818_1093+820del | |
ENST00000706903.1:c.*124+520_*124+522del | ENSP00000516614.1:n.*124+520_*124+522del | |
ENST00000706904.1:c.1093+818_1093+820del | ENSP00000516615.1:n.1093+818_1093+820del | |
ENST00000706905.1:c.*644_*646del | ENSP00000516616.1:n.*644_*646del |