HGVS | Genome Assembly |
---|---|
NC_000022.11:g.32050008dup , CM000684.2:g.32050008dup | GRCh38 |
NC_000022.10:g.32445995dup , CM000684.1:g.32445995dup | GRCh37 |
NC_000022.9:g.30775995dup | NCBI36 |
NG_017045.1:g.11977dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000266088.9:c.201dup MANE Select | ENSP00000266088.4:p.Trp68ValfsTer10 | |
ENST00000266088.8:c.201dup | ENSP00000266088.4:p.Trp68ValfsTer10 | |
NM_000343.3:c.201dup | NP_000334.1:p.Trp68ValfsTer10 | |
XM_011530331.1:c.201dup | XP_011528633.1:p.Trp68ValfsTer10 | |
NM_000343.4:c.201dup MANE Select | NP_000334.1:p.Trp68ValfsTer10 |