HGVS | Genome Assembly |
---|---|
NC_000015.10:g.34791123C>T , CM000677.2:g.34791123C>T | GRCh38 |
NC_000015.9:g.35083324C>T , CM000677.1:g.35083324C>T | GRCh37 |
NC_000015.8:g.32870616C>T | NCBI36 |
NG_007553.1:g.9604G>A , LRG_388:g.9604G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000560563.2:n.1881G>A (ACTC1) | ||
ENST00000290378.6:c.981G>A (ACTC1) MANE Select | ENSP00000290378.4:p.Met327Ile | |
ENST00000647798.1:n.1075G>A (ACTC1) | ||
ENST00000650163.1:n.1061G>A (ACTC1) | ||
ENST00000290378.4:c.981G>A (ACTC1) | ENSP00000290378.4:p.Met327Ile | |
NM_005159.4:c.981G>A , LRG_388t1:c.981G>A (ACTC1) | NP_005150.1:p.Met327Ile | |
NR_120329.1:n.299+13692C>T (GJD2-DT) | ||
NM_005159.5:c.981G>A (ACTC1) MANE Select | NP_005150.1:p.Met327Ile |