HGVS | Genome Assembly |
---|---|
NC_000016.10:g.173221C>A , CM000678.2:g.173221C>A | GRCh38 |
NC_000016.9:g.223220C>A , CM000678.1:g.223220C>A | GRCh37 |
NC_000016.8:g.163220C>A | NCBI36 |
NG_000006.1:g.34084C>A | |
NG_059186.1:g.1571C>A | |
NG_059271.1:g.5375C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000251595.11:c.192C>A MANE Select | ENSP00000251595.6:p.Ala64= | |
ENST00000251595.10:c.192C>A | ENSP00000251595.6:p.Ala64= | |
ENST00000397806.1:c.96C>A | ENSP00000380908.1:p.Ala32= | |
ENST00000482565.1:n.328C>A | ||
ENST00000484216.1:n.161C>A | ||
NM_000517.4:c.192C>A | NP_000508.1:p.Ala64= | |
NM_000517.6:c.192C>A MANE Select | NP_000508.1:p.Ala64= |