HGVS | Genome Assembly |
---|---|
NC_000006.12:g.32220587C= , CM000668.2:g.32220587C= | GRCh38 |
NC_000006.11:g.32188364C= , CM000668.1:g.32188364C= | GRCh37 |
NC_000006.10:g.32296342C= | NCBI36 |
NG_028190.1:g.8481G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000375023.3:c.977G= MANE Select | ENSP00000364163.3:p.Cys326= | |
ENST00000473562.1:n.1106G= | ||
NM_004557.3:c.977G= | NP_004548.3:p.Cys326= | |
NR_134949.1:n.1116G= | ||
NR_134950.1:n.1116G= | ||
NM_004557.4:c.977G= MANE Select | NP_004548.3:p.Cys326= | |
NR_134949.2:n.1116G= | ||
NR_134950.2:n.1116G= |