HGVS | Genome Assembly |
---|---|
NC_000015.10:g.34792144T>G , CM000677.2:g.34792144T>G | GRCh38 |
NC_000015.9:g.35084345T>G , CM000677.1:g.35084345T>G | GRCh37 |
NC_000015.8:g.32871637T>G | NCBI36 |
NG_007553.1:g.8583A>C , LRG_388:g.8583A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000560563.2:n.860A>C (ACTC1) | ||
ENST00000290378.6:c.754A>C (ACTC1) MANE Select | ENSP00000290378.4:p.Ile252Leu | |
ENST00000647798.1:n.848A>C (ACTC1) | ||
ENST00000650163.1:n.834A>C (ACTC1) | ||
ENST00000290378.4:c.754A>C (ACTC1) | ENSP00000290378.4:p.Ile252Leu | |
ENST00000557860.1:n.444A>C (ACTC1) | ||
ENST00000560563.1:n.253A>C (ACTC1) | ||
NM_005159.4:c.754A>C , LRG_388t1:c.754A>C (ACTC1) | NP_005150.1:p.Ile252Leu | |
NR_120329.1:n.299+14713T>G (GJD2-DT) | ||
NM_005159.5:c.754A>C (ACTC1) MANE Select | NP_005150.1:p.Ile252Leu |