HGVS | Genome Assembly |
---|---|
NC_000021.9:g.46001392del , CM000683.2:g.46001392del | GRCh38 |
NC_000021.8:g.47421306del , CM000683.1:g.47421306del | GRCh37 |
NC_000021.7:g.46245734del | NCBI36 |
NG_008674.1:g.24644del , LRG_475:g.24644del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000463060.6:n.355+6del | ||
ENST00000612273.2:c.82+6del | ||
ENST00000682634.1:c.82+6del | ||
ENST00000361866.8:c.1956+6del MANE Select | ENSP00000355180.3:n.1956+6del | |
ENST00000361866.7:c.1956+6del | ENSP00000355180.3:n.1956+6del | |
ENST00000463060.5:n.355+6del | ||
ENST00000498614.5:n.190+6del | ||
ENST00000612273.1:c.1950+6del | ENSP00000483630.1:n.1950+6del | |
NM_001848.2:c.1956+6del , LRG_475t1:c.1956+6del | NP_001839.2:n.1956+6del | |
NM_001848.3:c.1956+6del MANE Select | NP_001839.2:n.1956+6del |