HGVS | Genome Assembly |
---|---|
NC_000017.11:g.47286300G= , CM000679.2:g.47286300G= | GRCh38 |
NC_000017.10:g.45363666G= , CM000679.1:g.45363666G= | GRCh37 |
NC_000017.9:g.42718665G= | NCBI36 |
NG_008332.2:g.37459G= , LRG_481:g.37459G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696963.1:c.655G= | ENSP00000513002.1:p.Val219= | |
ENST00000559488.7:c.655G= MANE Select | ENSP00000452786.2:p.Val219= | |
ENST00000559488.5:c.655G= | ENSP00000452786.1:p.Val219= | |
ENST00000560629.1:c.620G= | ||
ENST00000571680.1:c.655G= | ENSP00000461626.1:p.Val219= | |
NM_000212.2:c.655G= , LRG_481t1:c.655G= | NP_000203.2:p.Val219= | |
NM_000212.3:c.655G= MANE Select | NP_000203.2:p.Val219= |