Canonical Allele Identifier:
CA1502599189
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.148649528T= , CM000666.2:g.148649528T= | GRCh38 |
| NC_000004.11:g.149570680T= , CM000666.1:g.149570680T= | GRCh37 |
| NC_000004.10:g.149790130T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_939336.1:n.437-30660A= | ||
| XR_001741441.1:n.1745+104944T= | ||
| XR_939336.3:n.2921-30660A= |