Linked Data
dbSNP Id:
rs2140428438
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.34789871C>A , CM000677.2:g.34789871C>A | GRCh38 |
| NC_000015.9:g.35082072C>A , CM000677.1:g.35082072C>A | GRCh37 |
| NC_000015.8:g.32869364C>A | NCBI36 |
| NG_007553.1:g.10856G>T , LRG_388:g.10856G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000290378.4:c.*541G>T (ACTC1) | ENSP00000290378.4:n.*541G>T | |
| NM_005159.4:c.*541G>T , LRG_388t1:c.*541G>T (ACTC1) | NP_005150.1:n.*541G>T | |
| NR_120329.1:n.299+12440C>A (GJD2-DT) |