HGVS | Genome Assembly |
---|---|
NC_000015.10:g.42958002_42958003del , CM000677.2:g.42958002_42958003del | GRCh38 |
NC_000015.9:g.43250200_43250201del , CM000677.1:g.43250200_43250201del | GRCh37 |
NC_000015.8:g.41037492_41037493del | NCBI36 |
NG_012182.1:g.153090_153091del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000290650.9:c.4835+14_4835+15del MANE Select | ENSP00000290650.4:n.4835+14_4835+15del | |
ENST00000290650.8:c.4835+14_4835+15del | ENSP00000290650.4:n.4835+14_4835+15del | |
NM_174916.2:c.4835+14_4835+15del | NP_777576.1:n.4835+14_4835+15del | |
NM_174916.3:c.4835+14_4835+15del MANE Select | NP_777576.1:n.4835+14_4835+15del |