HGVS | Genome Assembly |
---|---|
NC_000022.11:g.23834517_23834539dup , CM000684.2:g.23834517_23834539dup | GRCh38 |
NC_000022.10:g.24176704_24176726dup , CM000684.1:g.24176704_24176726dup | GRCh37 |
NC_000022.9:g.22506704_22506726dup | NCBI36 |
NG_009303.1:g.52555_52577dup , LRG_520:g.52555_52577dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000407422.8:c.*337_*359dup | ENSP00000383984.3:n.*337_*359dup | |
ENST00000644036.2:c.*337_*359dup MANE Select | ENSP00000494049.2:n.*337_*359dup | |
NM_001007468.3:c.*337_*359dup | NP_001007469.1:n.*337_*359dup | |
NM_001317946.2:c.*337_*359dup | NP_001304875.1:n.*337_*359dup | |
NM_001362877.2:c.*337_*359dup | NP_001349806.1:n.*337_*359dup | |
NM_003073.5:c.*337_*359dup MANE Select | NP_003064.2:n.*337_*359dup |