HGVS | Genome Assembly |
---|---|
NC_000001.11:g.94418439_94418444dup , CM000663.2:g.94418439_94418444dup | GRCh38 |
NC_000001.10:g.94883995_94884000dup , CM000663.1:g.94883995_94884000dup | GRCh37 |
NC_000001.9:g.94656583_94656588dup | NCBI36 |
NG_008865.1:g.5063_5068dup |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000370214.9:c.-40_-35dup MANE Select | ENSP00000359233.4:n.-40_-35dup | |
NM_001122674.1:c.-40_-35dup | NP_001116146.1:n.-40_-35dup | |
NM_002858.3:c.-40_-35dup | NP_002849.1:n.-40_-35dup | |
XM_006710802.2:c.-40_-35dup | XP_006710865.2:n.-40_-35dup | |
NM_002858.4:c.-40_-35dup MANE Select | NP_002849.1:n.-40_-35dup | |
NM_001122674.2:c.-40_-35dup | NP_001116146.1:n.-40_-35dup |