HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17401487dup , CM000663.2:g.17401487dup | GRCh38 |
NC_000001.10:g.17727983dup , CM000663.1:g.17727983dup | GRCh37 |
NC_000001.9:g.17600570dup | NCBI36 |
NG_032943.1:g.34242dup | |
NG_032943.2:g.34242dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000619609.1:c.*49dup MANE Select | ENSP00000483125.1:n.*49dup | |
NM_207421.4:c.*49dup MANE Select | NP_997304.3:n.*49dup |