HGVS | Genome Assembly |
---|---|
NC_000021.9:g.45987769_45987773del , CM000683.2:g.45987769_45987773del | GRCh38 |
NC_000021.8:g.47407683_47407687del , CM000683.1:g.47407683_47407687del | GRCh37 |
NC_000021.7:g.46232111_46232115del | NCBI36 |
NG_008674.1:g.11021_11025del , LRG_475:g.11021_11025del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361866.8:c.804+115_804+119del MANE Select | ENSP00000355180.3:n.804+115_804+119del | |
ENST00000361866.7:c.804+115_804+119del | ENSP00000355180.3:n.804+115_804+119del | |
ENST00000612273.1:c.804+115_804+119del | ENSP00000483630.1:n.804+115_804+119del | |
NM_001848.2:c.804+115_804+119del , LRG_475t1:c.804+115_804+119del | NP_001839.2:n.804+115_804+119del | |
NM_001848.3:c.804+115_804+119del MANE Select | NP_001839.2:n.804+115_804+119del |