HGVS | Genome Assembly |
---|---|
NC_000022.11:g.20888065_20888066del , CM000684.2:g.20888065_20888066del | GRCh38 |
NC_000022.10:g.21242353_21242354del , CM000684.1:g.21242353_21242354del | GRCh37 |
NC_000022.9:g.19572353_19572354del | NCBI36 |
NG_012152.1:g.34062_34063del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000215730.12:c.*229_*230del MANE Select | ENSP00000215730.6:n.*229_*230del | |
ENST00000215730.11:c.*229_*230del | ENSP00000215730.6:n.*229_*230del | |
NM_004782.3:c.*229_*230del | NP_004773.1:n.*229_*230del | |
NM_004782.4:c.*229_*230del MANE Select | NP_004773.1:n.*229_*230del |