HGVS | Genome Assembly |
---|---|
NC_000015.10:g.42958163_42958172del , CM000677.2:g.42958163_42958172del | GRCh38 |
NC_000015.9:g.43250361_43250370del , CM000677.1:g.43250361_43250370del | GRCh37 |
NC_000015.8:g.41037653_41037662del | NCBI36 |
NG_012182.1:g.152917_152926del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000290650.9:c.4758-82_4758-73del MANE Select | ENSP00000290650.4:n.4758-82_4758-73del | |
ENST00000290650.8:c.4758-82_4758-73del | ENSP00000290650.4:n.4758-82_4758-73del | |
NM_174916.2:c.4758-82_4758-73del | NP_777576.1:n.4758-82_4758-73del | |
NM_174916.3:c.4758-82_4758-73del MANE Select | NP_777576.1:n.4758-82_4758-73del |