HGVS | Genome Assembly |
---|---|
NC_000010.11:g.104034377_104034379del , CM000672.2:g.104034377_104034379del | GRCh38 |
NC_000010.10:g.105794135_105794137del , CM000672.1:g.105794135_105794137del | GRCh37 |
NC_000010.9:g.105784125_105784127del | NCBI36 |
NG_007069.1:g.56504_56506del |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000369733.8:c.3521-43_3521-41del | ENSP00000358748.3:n.3521-43_3521-41del | |
ENST00000648076.2:c.3767-43_3767-41del MANE Select | ENSP00000497653.1:n.3767-43_3767-41del | |
ENST00000353479.9:c.3767-43_3767-41del | ENSP00000340937.5:n.3767-43_3767-41del | |
ENST00000369733.7:c.3521-43_3521-41del | ENSP00000358748.3:n.3521-43_3521-41del | |
NM_000494.3:c.3767-43_3767-41del | NP_000485.3:n.3767-43_3767-41del | |
NM_000494.4:c.3767-43_3767-41del MANE Select | NP_000485.3:n.3767-43_3767-41del |