HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17401496dup , CM000663.2:g.17401496dup | GRCh38 |
NC_000001.10:g.17727992dup , CM000663.1:g.17727992dup | GRCh37 |
NC_000001.9:g.17600579dup | NCBI36 |
NG_032943.1:g.34251dup | |
NG_032943.2:g.34251dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000619609.1:c.*58dup MANE Select | ENSP00000483125.1:n.*58dup | |
NM_207421.4:c.*58dup MANE Select | NP_997304.3:n.*58dup |