HGVS | Genome Assembly |
---|---|
NC_000011.10:g.6319112A= , CM000673.2:g.6319112A= | GRCh38 |
NC_000011.9:g.6340342A= , CM000673.1:g.6340342A= | GRCh37 |
NC_000011.8:g.6296918A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303927.4:c.*51T= MANE Select | ENSP00000307292.3:n.*51T= | |
ENST00000303927.3:c.*51T= | ENSP00000307292.3:n.*51T= | |
ENST00000532354.1:n.859T= | ||
NM_145040.2:c.*51T= | NP_659477.2:n.*51T= | |
XR_930997.1:n.720+892A= | ||
NM_145040.3:c.*51T= MANE Select | NP_659477.2:n.*51T= |