Canonical Allele Identifier:
CA1481405665
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.102499749C= , CM000666.2:g.102499749C= | GRCh38 |
| NC_000004.11:g.103420906C= , CM000666.1:g.103420906C= | GRCh37 |
| NC_000004.10:g.103639938C= | NCBI36 |
| NG_050628.1:g.3421C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011532467.1:c.643+1500G= | XP_011530769.1:n.643+1500G= | |
| NR_136202.1:n.48+2690G= |