HGVS | Genome Assembly |
---|---|
NC_000016.10:g.11281348T= , CM000678.2:g.11281348T= | GRCh38 |
NC_000016.9:g.11375205T= , CM000678.1:g.11375205T= | GRCh37 |
NC_000016.8:g.11282706T= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000649869.1:n.152+31570T= (RMI2) | ||
ENST00000312511.3:c.-110A= (PRM1) | ENSP00000310515.3:n.-110A= | |
ENST00000572173.1:c.-515-13868T= (RMI2) | ENSP00000461206.1:n.-515-13868T= | |
ENST00000573910.1:n.160+31570T= (RMI2) | ||
XR_933070.1:n.733+31570T= | ||
XR_933070.3:n.876+31570T= |