HGVS | Genome Assembly |
---|---|
NC_000015.10:g.34794529T>A , CM000677.2:g.34794529T>A | GRCh38 |
NC_000015.9:g.35086730T>A , CM000677.1:g.35086730T>A | GRCh37 |
NC_000015.8:g.32874022T>A | NCBI36 |
NG_007553.1:g.6198A>T , LRG_388:g.6198A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000560563.2:n.235+151A>T (ACTC1) | ||
ENST00000290378.6:c.129+151A>T (ACTC1) MANE Select | ENSP00000290378.4:n.129+151A>T | |
ENST00000290378.4:c.129+151A>T (ACTC1) | ENSP00000290378.4:n.129+151A>T | |
NM_005159.4:c.129+151A>T , LRG_388t1:c.129+151A>T (ACTC1) | NP_005150.1:n.129+151A>T | |
NR_120329.1:n.300-15967T>A (GJD2-DT) | ||
NM_005159.5:c.129+151A>T (ACTC1) MANE Select | NP_005150.1:n.129+151A>T |