HGVS | Genome Assembly |
---|---|
NC_000015.10:g.34791581G>T , CM000677.2:g.34791581G>T | GRCh38 |
NC_000015.9:g.35083782G>T , CM000677.1:g.35083782G>T | GRCh37 |
NC_000015.8:g.32871074G>T | NCBI36 |
NG_007553.1:g.9146C>A , LRG_388:g.9146C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000560563.2:n.1423C>A (ACTC1) | ||
ENST00000290378.6:c.809-286C>A (ACTC1) MANE Select | ENSP00000290378.4:n.809-286C>A | |
ENST00000647798.1:n.903-286C>A (ACTC1) | ||
ENST00000650163.1:n.889-286C>A (ACTC1) | ||
ENST00000290378.4:c.809-286C>A (ACTC1) | ENSP00000290378.4:n.809-286C>A | |
ENST00000557860.1:n.499-286C>A (ACTC1) | ||
NM_005159.4:c.809-286C>A , LRG_388t1:c.809-286C>A (ACTC1) | NP_005150.1:n.809-286C>A | |
NR_120329.1:n.299+14150G>T (GJD2-DT) | ||
NM_005159.5:c.809-286C>A (ACTC1) MANE Select | NP_005150.1:n.809-286C>A |