HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45987786_45987787delinsCG , CM000683.2:g.45987786_45987787delinsCG | GRCh38 |
NC_000021.8:g.47407700_47407701delinsCG , CM000683.1:g.47407700_47407701delinsCG | GRCh37 |
NC_000021.7:g.46232128_46232129delinsCG | NCBI36 |
NG_008674.1:g.11038_11039delinsCG , LRG_475:g.11038_11039delinsCG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.804+132_804+133delinsCG MANE Select | ENSP00000355180.3:n.804+132_804+133delinsCG | |
ENST00000361866.7:c.804+132_804+133delinsCG | ENSP00000355180.3:n.804+132_804+133delinsCG | |
ENST00000612273.1:c.804+132_804+133delinsCG | ENSP00000483630.1:n.804+132_804+133delinsCG | |
NM_001848.2:c.804+132_804+133delinsCG , LRG_475t1:c.804+132_804+133delinsCG | NP_001839.2:n.804+132_804+133delinsCG | |
NM_001848.3:c.804+132_804+133delinsCG MANE Select | NP_001839.2:n.804+132_804+133delinsCG |