HGVS | Genome Assembly |
---|---|
NC_000017.11:g.41586762dup , CM000679.2:g.41586762dup | GRCh38 |
NC_000017.10:g.39743014dup , CM000679.1:g.39743014dup | GRCh37 |
NC_000017.9:g.36996540dup | NCBI36 |
NG_008624.1:g.5138dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000167586.7:c.77dup MANE Select | ENSP00000167586.6:p.Gly27ArgfsTer? | |
ENST00000167586.6:c.77dup | ENSP00000167586.6:p.Gly27ArgfsTer? | |
NM_000526.4:c.77dup | NP_000517.2:p.Gly27ArgfsTer? | |
NM_000526.5:c.77dup MANE Select | NP_000517.3:p.Gly27ArgfsTer? |