Canonical Allele Identifier:
CA1496030179
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.134601585C= , CM000666.2:g.134601585C= | GRCh38 |
| NC_000004.11:g.135522740C= , CM000666.1:g.135522740C= | GRCh37 |
| NC_000004.10:g.135742190C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_939212.1:n.410+14226C= | |
| XR_939214.1:n.392+14226C= | |
| XR_939214.2:n.392+14226C= |