HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5233056T>C , CM000673.2:g.5233056T>C | GRCh38 |
NC_000011.9:g.5254286T>C , CM000673.1:g.5254286T>C | GRCh37 |
NC_000011.8:g.5210862T>C | NCBI36 |
NG_000007.3:g.64560A>G | |
NG_063112.2:g.15602A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000643122.1:c.352A>G | ENSP00000494708.1:p.Asn118Asp | |
ENST00000650601.1:c.352A>G MANE Select | ENSP00000497529.1:p.Asn118Asp | |
ENST00000292901.7:c.316-258A>G | ENSP00000292901.3:n.316-258A>G | |
ENST00000380299.3:c.352A>G | ENSP00000369654.3:p.Asn118Asp | |
ENST00000417377.1:c.129A>G | ENSP00000414741.1:p.Ala43= | |
NM_000519.3:c.352A>G | NP_000510.1:p.Asn118Asp | |
NM_000519.4:c.352A>G MANE Select | NP_000510.1:p.Asn118Asp |