HGVS | Genome Assembly |
---|---|
NC_000005.10:g.1213312_1213424del , CM000667.2:g.1213312_1213424del | GRCh38 |
NC_000005.9:g.1213427_1213539del , CM000667.1:g.1213427_1213539del | GRCh37 |
NC_000005.8:g.1266427_1266539del | NCBI36 |
NG_008282.1:g.16718_16830del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000304460.11:c.664-151_664-39del MANE Select | ENSP00000305302.10:n.664-151_664-39del | |
ENST00000304460.10:c.664-151_664-39del | ENSP00000305302.10:n.664-151_664-39del | |
ENST00000515652.5:c.572-151_572-39del | ENSP00000425701.1:n.572-151_572-39del | |
NM_001003841.2:c.664-151_664-39del | NP_001003841.1:n.664-151_664-39del | |
NM_001003841.3:c.664-151_664-39del MANE Select | NP_001003841.1:n.664-151_664-39del |