HGVS | Genome Assembly |
---|---|
NC_000023.11:g.48523780C>A , CM000685.2:g.48523780C>A | GRCh38 |
NC_000023.10:g.48382168C>A , CM000685.1:g.48382168C>A | GRCh37 |
NC_000023.9:g.48267112C>A | NCBI36 |
NG_007452.1:g.7005C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000495186.6:c.9C>A MANE Select | ENSP00000417052.1:p.Thr3= | |
ENST00000651615.1:c.9C>A | ENSP00000498524.1:p.Thr3= | |
ENST00000276096.10:n.110-143C>A | ||
ENST00000414061.1:c.9C>A | ENSP00000405832.1:p.Thr3= | |
ENST00000446158.5:c.9C>A | ENSP00000390031.1:p.Thr3= | |
ENST00000495186.5:c.9C>A | ENSP00000417052.1:p.Thr3= | |
ENST00000498425.1:n.130C>A | ||
NM_006579.2:c.9C>A | NP_006570.1:p.Thr3= | |
NM_006579.3:c.9C>A MANE Select | NP_006570.1:p.Thr3= |