HGVS | Genome Assembly |
---|---|
NC_000011.10:g.6319143G= , CM000673.2:g.6319143G= | GRCh38 |
NC_000011.9:g.6340373G= , CM000673.1:g.6340373G= | GRCh37 |
NC_000011.8:g.6296949G= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000303927.4:c.*20C= MANE Select | ENSP00000307292.3:n.*20C= | |
ENST00000303927.3:c.*20C= | ENSP00000307292.3:n.*20C= | |
ENST00000524852.1:n.592C= | ||
ENST00000532354.1:n.828C= | ||
NM_145040.2:c.*20C= | NP_659477.2:n.*20C= | |
XR_930997.1:n.720+923G= | ||
XR_242848.4:n.3G= | ||
NM_145040.3:c.*20C= MANE Select | NP_659477.2:n.*20C= |