HGVS | Genome Assembly |
---|---|
NC_000015.10:g.34790246G>A , CM000677.2:g.34790246G>A | GRCh38 |
NC_000015.9:g.35082447G>A , CM000677.1:g.35082447G>A | GRCh37 |
NC_000015.8:g.32869739G>A | NCBI36 |
NG_007553.1:g.10481C>T , LRG_388:g.10481C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000560563.2:n.2200C>T (ACTC1) | ||
ENST00000290378.6:c.*166C>T (ACTC1) MANE Select | ENSP00000290378.4:n.*166C>T | |
ENST00000647798.1:n.1394C>T (ACTC1) | ||
ENST00000650163.1:n.1380C>T (ACTC1) | ||
ENST00000290378.4:c.*166C>T (ACTC1) | ENSP00000290378.4:n.*166C>T | |
NM_005159.4:c.*166C>T , LRG_388t1:c.*166C>T (ACTC1) | NP_005150.1:n.*166C>T | |
NR_120329.1:n.299+12815G>A (GJD2-DT) | ||
NM_005159.5:c.*166C>T (ACTC1) MANE Select | NP_005150.1:n.*166C>T |