HGVS | Genome Assembly |
---|---|
NC_000001.11:g.17401083_17401084dup , CM000663.2:g.17401083_17401084dup | GRCh38 |
NC_000001.10:g.17727579_17727580dup , CM000663.1:g.17727579_17727580dup | GRCh37 |
NC_000001.9:g.17600166_17600167dup | NCBI36 |
NG_032943.1:g.33838_33839dup | |
NG_032943.2:g.33838_33839dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000619609.1:c.1852-122_1852-121dup MANE Select | ENSP00000483125.1:n.1852-122_1852-121dup | |
NM_207421.4:c.1852-122_1852-121dup MANE Select | NP_997304.3:n.1852-122_1852-121dup |