HGVS | Genome Assembly |
---|---|
NC_000001.11:g.161306108del , CM000663.2:g.161306108del | GRCh38 |
NC_000001.10:g.161275898del , CM000663.1:g.161275898del | GRCh37 |
NC_000001.9:g.159542522del | NCBI36 |
NG_008055.1:g.8866del , LRG_256:g.8866del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000526189.3:c.564+1del | ||
ENST00000533357.5:c.645+1del | ||
ENST00000672287.2:c.57+1del | ||
ENST00000672602.2:c.645+1del | ||
ENST00000674861.1:n.708+1del | ||
ENST00000463290.5:c.645+1del | ||
ENST00000476410.1:n.106del | ||
ENST00000488271.1:n.83+1del | ||
ENST00000491222.5:c.57+1del | ||
ENST00000526189.2:c.308+1del | ||
ENST00000533357.4:c.645+1del | ||
NM_000530.6:c.645+1del , LRG_256t1:c.645+1del | ||
NM_000530.7:c.645+1del | ||
NM_001315491.1:c.645+1del | ||
XM_017001321.2:c.675+1del | ||
NM_000530.8:c.645+1del | ||
NM_001315491.2:c.645+1del |