HGVS | Genome Assembly |
---|---|
NC_000001.11:g.229431495dup , CM000663.2:g.229431495dup | GRCh38 |
NC_000001.10:g.229567242dup , CM000663.1:g.229567242dup | GRCh37 |
NC_000001.9:g.227633865dup | NCBI36 |
NG_006672.1:g.7602dup , LRG_429:g.7602dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000366683.4:c.*4dup | ENSP00000355644.4:n.*4dup | |
ENST00000684723.1:c.*4dup | ENSP00000508084.1:n.*4dup | |
ENST00000366683.3:c.*4dup | ENSP00000355644.3:n.*4dup | |
ENST00000366684.7:c.*4dup MANE Select | ENSP00000355645.3:n.*4dup | |
NM_001100.3:c.*4dup , LRG_429t1:c.*4dup | NP_001091.1:n.*4dup | |
NM_001100.4:c.*4dup MANE Select | NP_001091.1:n.*4dup |