Canonical Allele Identifier:
CA2762880458
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.102499860A>C , CM000666.2:g.102499860A>C | GRCh38 |
| NC_000004.11:g.103421017A>C , CM000666.1:g.103421017A>C | GRCh37 |
| NC_000004.10:g.103640049A>C | NCBI36 |
| NG_050628.1:g.3532A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011532467.1:c.643+1389T>G | XP_011530769.1:n.643+1389T>G | |
| NR_136202.1:n.48+2579T>G |