HGVS | Genome Assembly |
---|---|
NC_000015.10:g.34790368A= , CM000677.2:g.34790368A= | GRCh38 |
NC_000015.9:g.35082569A= , CM000677.1:g.35082569A= | GRCh37 |
NC_000015.8:g.32869861A= | NCBI36 |
NG_007553.1:g.10359T= , LRG_388:g.10359T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000560563.2:n.2078T= (ACTC1) | ||
ENST00000290378.6:c.*44T= (ACTC1) MANE Select | ENSP00000290378.4:n.*44T= | |
ENST00000647798.1:n.1272T= (ACTC1) | ||
ENST00000650163.1:n.1258T= (ACTC1) | ||
ENST00000290378.4:c.*44T= (ACTC1) | ENSP00000290378.4:n.*44T= | |
NM_005159.4:c.*44T= , LRG_388t1:c.*44T= (ACTC1) | NP_005150.1:n.*44T= | |
NR_120329.1:n.299+12937A= (GJD2-DT) | ||
NM_005159.5:c.*44T= (ACTC1) MANE Select | NP_005150.1:n.*44T= |