HGVS | Genome Assembly |
---|---|
NC_000015.10:g.34792540T>C , CM000677.2:g.34792540T>C | GRCh38 |
NC_000015.9:g.35084741T>C , CM000677.1:g.35084741T>C | GRCh37 |
NC_000015.8:g.32872033T>C | NCBI36 |
NG_007553.1:g.8187A>G , LRG_388:g.8187A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000560563.2:n.590A>G (ACTC1) | ||
ENST00000290378.6:c.484A>G (ACTC1) MANE Select | ENSP00000290378.4:p.Thr162Ala | |
ENST00000647798.1:n.578A>G (ACTC1) | ||
ENST00000648556.1:n.641A>G (ACTC1) | ||
ENST00000650163.1:n.564A>G (ACTC1) | ||
ENST00000290378.4:c.484A>G (ACTC1) | ENSP00000290378.4:p.Thr162Ala | |
ENST00000557860.1:n.174A>G (ACTC1) | ||
NM_005159.4:c.484A>G , LRG_388t1:c.484A>G (ACTC1) | NP_005150.1:p.Thr162Ala | |
NR_120329.1:n.299+15109T>C (GJD2-DT) | ||
NM_005159.5:c.484A>G (ACTC1) MANE Select | NP_005150.1:p.Thr162Ala |