Linked Data
ClinVar Variation Id:
384419
dbSNP Id:
rs779757924
ExAC:
10:90703627 G / C
gnomAD v2:
10-90703627-G-C
gnomAD v3:
10-88943870-G-C
gnomAD v4:
10-88943870-G-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.88943870G>C , CM000672.2:g.88943870G>C | GRCh38 |
| NC_000010.10:g.90703627G>C , CM000672.1:g.90703627G>C | GRCh37 |
| NC_000010.9:g.90693607G>C | NCBI36 |
| NG_011541.1:g.52521C>G , LRG_781:g.52521C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000415557.2:c.296C>G (ACTA2) | ENSP00000396730.2:p.Ala99Gly | |
| ENST00000458159.6:c.296C>G (ACTA2) | ENSP00000398239.2:p.Ala99Gly | |
| ENST00000480297.6:n.362C>G (ACTA2) | ||
| ENST00000482085.2:n.1777C>G (ACTA2) | ||
| ENST00000224784.10:c.296C>G (ACTA2) MANE Select | ENSP00000224784.6:p.Ala99Gly | |
| ENST00000371927.7:c.1254+21434G>C (STAMBPL1) | ENSP00000360995.3:n.1254+21434G>C | |
| ENST00000415557.1:c.296C>G (ACTA2) | ENSP00000396730.1:p.Ala99Gly | |
| ENST00000458159.5:c.296C>G (ACTA2) | ENSP00000398239.1:p.Ala99Gly | |
| ENST00000458208.5:c.296C>G (ACTA2) | ENSP00000402373.1:p.Ala99Gly | |
| ENST00000480297.5:n.336C>G (ACTA2) | ||
| NM_001141945.1:c.296C>G , LRG_781t2:c.296C>G (ACTA2) | NP_001135417.1:p.Ala99Gly | |
| NM_001613.2:c.296C>G , LRG_781t1:c.296C>G (ACTA2) | NP_001604.1:p.Ala99Gly | |
| XM_011540016.1:c.296C>G (ACTA2) | XP_011538318.1:p.Ala99Gly | |
| NM_001141945.2:c.296C>G (ACTA2) | NP_001135417.1:p.Ala99Gly | |
| NM_001320855.1:c.296C>G (ACTA2) | NP_001307784.1:p.Ala99Gly | |
| NM_001613.3:c.296C>G (ACTA2) | NP_001604.1:p.Ala99Gly | |
| NM_001613.4:c.296C>G (ACTA2) MANE Select | NP_001604.1:p.Ala99Gly |