HGVS | Genome Assembly |
---|---|
NC_000001.11:g.114714018_114714019insGGGGCCAGGGTGGTAGGGAAG , CM000663.2:g.114714018_114714019insGGGGCCAGGGTGGTAGGGAAG | GRCh38 |
NC_000001.10:g.115256639_115256640insGGGGCCAGGGTGGTAGGGAAG , CM000663.1:g.115256639_115256640insGGGGCCAGGGTGGTAGGGAAG | GRCh37 |
NC_000001.9:g.115058162_115058163insGGGGCCAGGGTGGTAGGGAAG | NCBI36 |
NG_007572.1:g.7883_7884insACCACCCTGGCCCCCTTCCCT , LRG_92:g.7883_7884insACCACCCTGGCCCCCTTCCCT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369535.5:c.112-34_112-33insACCACCCTGGCCCCCTTCCCT MANE Select | ENSP00000358548.4:n.112-34_112-33insACCACCCTGGCCCCCTTCCCT | |
ENST00000369535.4:c.112-34_112-33insACCACCCTGGCCCCCTTCCCT | ENSP00000358548.4:n.112-34_112-33insACCACCCTGGCCCCCTTCCCT | |
NM_002524.4:c.112-34_112-33insACCACCCTGGCCCCCTTCCCT | NP_002515.1:n.112-34_112-33insACCACCCTGGCCCCCTTCCCT | |
NM_002524.5:c.112-34_112-33insACCACCCTGGCCCCCTTCCCT MANE Select | NP_002515.1:n.112-34_112-33insACCACCCTGGCCCCCTTCCCT |