Linked Data
gnomAD v4:
11-47582327-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.47582327T>C , CM000673.2:g.47582327T>C | GRCh38 |
| NC_000011.9:g.47603879T>C , CM000673.1:g.47603879T>C | GRCh37 |
| NC_000011.8:g.47560455T>C | NCBI36 |
| NG_011946.1:g.8318T>C | |
| NG_011946.2:g.8318T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263774.9:c.508-22T>C MANE Select | ENSP00000263774.4:n.508-22T>C | |
| ENST00000531351.2:n.1681T>C | ||
| ENST00000677462.1:n.2982-22T>C | ||
| ENST00000678975.1:n.2765-22T>C | ||
| ENST00000263774.8:c.508-22T>C | ENSP00000263774.4:n.508-22T>C | |
| ENST00000524568.1:n.611-22T>C | ||
| ENST00000525212.1:n.163-22T>C | ||
| ENST00000525378.5:n.446-22T>C | ||
| ENST00000527178.1:n.86T>C | ||
| ENST00000533507.5:n.1402-22T>C | ||
| NM_004551.2:c.508-22T>C | NP_004542.1:n.508-22T>C | |
| NM_004551.3:c.508-22T>C MANE Select | NP_004542.1:n.508-22T>C |