HGVS | Genome Assembly |
---|---|
NC_000018.10:g.77268539_77268548delinsACCGCCTCCT , CM000680.2:g.77268539_77268548delinsACCGCCTCCT | GRCh38 |
NC_000018.9:g.74980495_74980504delinsACCGCCTCCT , CM000680.1:g.74980495_74980504delinsACCGCCTCCT | GRCh37 |
NC_000018.8:g.73109483_73109492delinsACCGCCTCCT | NCBI36 |
NG_009223.1:g.23488_23497delinsACCGCCTCCT |
HGVS | Amino-acid change | |
---|---|---|
ENST00000299727.5:c.733-46_733-37delinsACCGCCTCCT MANE Select | ENSP00000299727.3:n.733-46_733-37delinsAC... | |
ENST00000299727.4:c.733-46_733-37delinsACCGCCTCCT | ENSP00000299727.3:n.733-46_733-37delinsAC... | |
NM_001480.3:c.733-46_733-37delinsACCGCCTCCT | NP_001471.2:n.733-46_733-37delinsACCGCCTC... | |
NM_001480.4:c.733-46_733-37delinsACCGCCTCCT MANE Select | NP_001471.2:n.733-46_733-37delinsACCGCCTC... |