HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114714018_114714019insGGGGCCTGGGTGGGTGGGAAG , CM000663.2:g.114714018_114714019insGGGGCCTGGGTGGGTGGGAAG | GRCh38 |
NC_000001.10:g.115256639_115256640insGGGGCCTGGGTGGGTGGGAAG , CM000663.1:g.115256639_115256640insGGGGCCTGGGTGGGTGGGAAG | GRCh37 |
NC_000001.9:g.115058162_115058163insGGGGCCTGGGTGGGTGGGAAG | NCBI36 |
NG_007572.1:g.7882_7883insACCCACCCAGGCCCCCTTCCC , LRG_92:g.7882_7883insACCCACCCAGGCCCCCTTCCC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.112-35_112-34insACCCACCCAGGCCCCCTTCCC MANE Select | ENSP00000358548.4:n.112-35_112-34insACCCACCCAGGCCCCCTTCCC | |
ENST00000369535.4:c.112-35_112-34insACCCACCCAGGCCCCCTTCCC | ENSP00000358548.4:n.112-35_112-34insACCCACCCAGGCCCCCTTCCC | |
NM_002524.4:c.112-35_112-34insACCCACCCAGGCCCCCTTCCC | NP_002515.1:n.112-35_112-34insACCCACCCAGGCCCCCTTCCC | |
NM_002524.5:c.112-35_112-34insACCCACCCAGGCCCCCTTCCC MANE Select | NP_002515.1:n.112-35_112-34insACCCACCCAGGCCCCCTTCCC |