HGVS | Genome Assembly |
---|---|
NC_000011.10:g.47582350T>G , CM000673.2:g.47582350T>G | GRCh38 |
NC_000011.9:g.47603902T>G , CM000673.1:g.47603902T>G | GRCh37 |
NC_000011.8:g.47560478T>G | NCBI36 |
NG_011946.1:g.8341T>G | |
NG_011946.2:g.8341T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000263774.9:c.509T>G MANE Select | ENSP00000263774.4:p.Ile170Ser | |
ENST00000531351.2:n.1704T>G | ||
ENST00000677462.1:n.2983T>G | ||
ENST00000678975.1:n.2766T>G | ||
ENST00000263774.8:c.509T>G | ENSP00000263774.4:p.Ile170Ser | |
ENST00000524568.1:n.612T>G | ||
ENST00000525212.1:n.164T>G | ||
ENST00000525378.5:n.447T>G | ||
ENST00000527178.1:n.109T>G | ||
ENST00000533507.5:n.1403T>G | ||
NM_004551.2:c.509T>G | NP_004542.1:p.Ile170Ser | |
NM_004551.3:c.509T>G MANE Select | NP_004542.1:p.Ile170Ser |