HGVS | Genome Assembly |
---|---|
NC_000017.11:g.47286416C>A , CM000679.2:g.47286416C>A | GRCh38 |
NC_000017.10:g.45363782C>A , CM000679.1:g.45363782C>A | GRCh37 |
NC_000017.9:g.42718781C>A | NCBI36 |
NG_008332.2:g.37575C>A , LRG_481:g.37575C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000696963.1:c.771C>A | ENSP00000513002.1:p.Val257= | |
ENST00000559488.7:c.771C>A MANE Select | ENSP00000452786.2:p.Val257= | |
ENST00000559488.5:c.771C>A | ENSP00000452786.1:p.Val257= | |
ENST00000560629.1:c.736C>A | ||
ENST00000571680.1:c.771C>A | ENSP00000461626.1:p.Val257= | |
NM_000212.2:c.771C>A , LRG_481t1:c.771C>A | NP_000203.2:p.Val257= | |
NM_000212.3:c.771C>A MANE Select | NP_000203.2:p.Val257= |