HGVS | Genome Assembly |
---|---|
NC_000005.10:g.63962176_63962248del , CM000667.2:g.63962176_63962248del | GRCh38 |
NC_000005.9:g.63258003_63258075del , CM000667.1:g.63258003_63258075del | GRCh37 |
NC_000005.8:g.63293759_63293831del | NCBI36 |
NG_032816.1:g.5053_5125del |
HGVS | Amino-acid change | |
---|---|---|
ENST00000323865.5:c.-521_-449del MANE Select | ENSP00000316244.4:n.-521_-449del | |
ENST00000506598.1:c.-387-134_-387-62del | ENSP00000423433.1:n.-387-134_-387-62del | |
NM_000524.3:c.-521_-449del | NP_000515.2:n.-521_-449del | |
NM_000524.4:c.-521_-449del MANE Select | NP_000515.2:n.-521_-449del |