HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45987793_45987795del , CM000683.2:g.45987793_45987795del | GRCh38 |
NC_000021.8:g.47407707_47407709del , CM000683.1:g.47407707_47407709del | GRCh37 |
NC_000021.7:g.46232135_46232137del | NCBI36 |
NG_008674.1:g.11045_11047del , LRG_475:g.11045_11047del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.804+139_804+141del MANE Select | ENSP00000355180.3:n.804+139_804+141del | |
ENST00000361866.7:c.804+139_804+141del | ENSP00000355180.3:n.804+139_804+141del | |
ENST00000612273.1:c.804+139_804+141del | ENSP00000483630.1:n.804+139_804+141del | |
NM_001848.2:c.804+139_804+141del , LRG_475t1:c.804+139_804+141del | NP_001839.2:n.804+139_804+141del | |
NM_001848.3:c.804+139_804+141del MANE Select | NP_001839.2:n.804+139_804+141del |