HGVS | Genome Assembly |
---|---|
NC_000015.10:g.34791250A>G , CM000677.2:g.34791250A>G | GRCh38 |
NC_000015.9:g.35083451A>G , CM000677.1:g.35083451A>G | GRCh37 |
NC_000015.8:g.32870743A>G | NCBI36 |
NG_007553.1:g.9477T>C , LRG_388:g.9477T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000560563.2:n.1754T>C (ACTC1) | ||
ENST00000290378.6:c.854T>C (ACTC1) MANE Select | ENSP00000290378.4:p.Met285Thr | |
ENST00000647798.1:n.948T>C (ACTC1) | ||
ENST00000650163.1:n.934T>C (ACTC1) | ||
ENST00000290378.4:c.854T>C (ACTC1) | ENSP00000290378.4:p.Met285Thr | |
ENST00000557860.1:n.544T>C (ACTC1) | ||
NM_005159.4:c.854T>C , LRG_388t1:c.854T>C (ACTC1) | NP_005150.1:p.Met285Thr | |
NR_120329.1:n.299+13819A>G (GJD2-DT) | ||
NM_005159.5:c.854T>C (ACTC1) MANE Select | NP_005150.1:p.Met285Thr |