Canonical Allele Identifier:
CA1481406828
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.102500892C= , CM000666.2:g.102500892C= | GRCh38 |
| NC_000004.11:g.103422049C= , CM000666.1:g.103422049C= | GRCh37 |
| NC_000004.10:g.103641081C= | NCBI36 |
| NG_050628.1:g.4564C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011532467.1:c.643+357G= | XP_011530769.1:n.643+357G= | |
| NR_136202.1:n.48+1547G= |