HGVS | Genome Assembly |
---|---|
NC_000016.10:g.173122C>G , CM000678.2:g.173122C>G | GRCh38 |
NC_000016.9:g.223121C>G , CM000678.1:g.223121C>G | GRCh37 |
NC_000016.8:g.163121C>G | NCBI36 |
NG_000006.1:g.33985C>G | |
NG_059186.1:g.1472C>G | |
NG_059271.1:g.5276C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000251595.11:c.96-3C>G MANE Select | ENSP00000251595.6:n.96-3C>G | |
ENST00000251595.10:c.96-3C>G | ENSP00000251595.6:n.96-3C>G | |
ENST00000397806.1:c.-1-3C>G | ENSP00000380908.1:n.-1-3C>G | |
ENST00000482565.1:n.229C>G | ||
ENST00000484216.1:n.65-3C>G | ||
NM_000517.4:c.96-3C>G | NP_000508.1:n.96-3C>G | |
NM_000517.6:c.96-3C>G MANE Select | NP_000508.1:n.96-3C>G |