Canonical Allele Identifier:
CA1595159117
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159580771C= , CM000667.2:g.159580771C= | GRCh38 |
| NC_000005.9:g.159007779C= , CM000667.1:g.159007779C= | GRCh37 |
| NC_000005.8:g.158940357C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_941139.1:n.2075+336C= | ||
| XR_941140.1:n.2075+336C= | ||
| XR_941141.1:n.570+336C= | ||
| XR_941139.2:n.2229+336C= |