HGVS | Genome Assembly |
---|---|
NC_000011.10:g.6319017C= , CM000673.2:g.6319017C= | GRCh38 |
NC_000011.9:g.6340247C= , CM000673.1:g.6340247C= | GRCh37 |
NC_000011.8:g.6296823C= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303927.4:c.*146G= MANE Select | ENSP00000307292.3:n.*146G= | |
ENST00000303927.3:c.*146G= | ENSP00000307292.3:n.*146G= | |
ENST00000532354.1:n.954G= | ||
NM_145040.2:c.*146G= | NP_659477.2:n.*146G= | |
XR_930997.1:n.720+797C= | ||
NM_145040.3:c.*146G= MANE Select | NP_659477.2:n.*146G= |