HGVS | Genome Assembly |
---|---|
NC_000016.10:g.173311G= , CM000678.2:g.173311G= | GRCh38 |
NC_000016.9:g.223310G= , CM000678.1:g.223310G= | GRCh37 |
NC_000016.8:g.163310G= | NCBI36 |
NG_000006.1:g.34174G= | |
NG_059186.1:g.1661G= | |
NG_059271.1:g.5465G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000251595.11:c.282G= MANE Select | ENSP00000251595.6:p.Val94= | |
ENST00000251595.10:c.282G= | ENSP00000251595.6:p.Val94= | |
ENST00000397806.1:c.186G= | ENSP00000380908.1:p.Val62= | |
ENST00000482565.1:n.418G= | ||
ENST00000484216.1:n.251G= | ||
NM_000517.4:c.282G= | NP_000508.1:p.Val94= | |
NM_000517.6:c.282G= MANE Select | NP_000508.1:p.Val94= |