Canonical Allele Identifier:
CA1734068788
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.110407414C= , CM000669.2:g.110407414C= | GRCh38 |
| NC_000007.13:g.110047471C= , CM000669.1:g.110047471C= | GRCh37 |
| NC_000007.12:g.109834707C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001744982.1:n.604+25397G= | ||
| XR_927863.2:n.367+25397G= |