HGVS | Genome Assembly |
---|---|
NC_000023.11:g.38403659C>A , CM000685.2:g.38403659C>A | GRCh38 |
NC_000023.10:g.38262912C>A , CM000685.1:g.38262912C>A | GRCh37 |
NC_000023.9:g.38147856C>A | NCBI36 |
NG_008471.1:g.56177C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000039007.5:c.582C>A MANE Select | ENSP00000039007.4:p.Ile194= | |
ENST00000643344.1:c.*332C>A | ENSP00000496606.1:n.*332C>A | |
ENST00000039007.4:c.582C>A | ENSP00000039007.4:p.Ile194= | |
ENST00000465127.1:c.172-262462C>A | ENSP00000417050.1:n.172-262462C>A | |
ENST00000488812.1:n.619C>A | ||
NM_000531.5:c.582C>A | NP_000522.3:p.Ile194= | |
XM_017029556.1:c.582C>A | XP_016885045.1:p.Ile194= | |
NM_000531.6:c.582C>A MANE Select | NP_000522.3:p.Ile194= |