HGVS | Genome Assembly |
---|---|
NC_000015.10:g.73322467dup , CM000677.2:g.73322467dup | GRCh38 |
NC_000015.9:g.73614808dup , CM000677.1:g.73614808dup | GRCh37 |
NC_000015.8:g.71401861dup | NCBI36 |
NG_009063.1:g.51799dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000261917.4:c.*15dup MANE Select | ENSP00000261917.3:n.*15dup | |
ENST00000261917.3:c.*15dup | ENSP00000261917.3:n.*15dup | |
NM_005477.2:c.*15dup | NP_005468.1:n.*15dup | |
XM_011521148.1:c.*15dup | XP_011519450.1:n.*15dup | |
XM_011521148.2:c.*15dup | XP_011519450.1:n.*15dup | |
NM_005477.3:c.*15dup MANE Select | NP_005468.1:n.*15dup |