HGVS | Genome Assembly |
---|---|
NC_000015.10:g.34792113G>A , CM000677.2:g.34792113G>A | GRCh38 |
NC_000015.9:g.35084314G>A , CM000677.1:g.35084314G>A | GRCh37 |
NC_000015.8:g.32871606G>A | NCBI36 |
NG_007553.1:g.8614C>T , LRG_388:g.8614C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000560563.2:n.891C>T (ACTC1) | ||
ENST00000290378.6:c.785C>T (ACTC1) MANE Select | ENSP00000290378.4:p.Thr262Ile | |
ENST00000647798.1:n.879C>T (ACTC1) | ||
ENST00000650163.1:n.865C>T (ACTC1) | ||
ENST00000290378.4:c.785C>T (ACTC1) | ENSP00000290378.4:p.Thr262Ile | |
ENST00000557860.1:n.475C>T (ACTC1) | ||
ENST00000560563.1:n.284C>T (ACTC1) | ||
NM_005159.4:c.785C>T , LRG_388t1:c.785C>T (ACTC1) | NP_005150.1:p.Thr262Ile | |
NR_120329.1:n.299+14682G>A (GJD2-DT) | ||
NM_005159.5:c.785C>T (ACTC1) MANE Select | NP_005150.1:p.Thr262Ile |