HGVS | Genome Assembly |
---|---|
NC_000006.12:g.1610017_1610029dup , CM000668.2:g.1610017_1610029dup | GRCh38 |
NC_000006.11:g.1610252_1610264dup , CM000668.1:g.1610252_1610264dup | GRCh37 |
NC_000006.10:g.1555251_1555263dup | NCBI36 |
NG_009368.1:g.4572_4584dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000645831.2:c.-429_-417dup MANE Select | ENSP00000493906.1:n.-429_-417dup | |
ENST00000380874.3:c.-429_-417dup | ENSP00000370256.2:n.-429_-417dup | |
NM_001453.3:c.-429_-417dup MANE Select | NP_001444.2:n.-429_-417dup |