Canonical Allele Identifier:
CA1610684712
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.11943349T= , CM000668.2:g.11943349T= | GRCh38 |
| NC_000006.11:g.11943582T= , CM000668.1:g.11943582T= | GRCh37 |
| NC_000006.10:g.12051568T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001743976.1:n.348-8186T= |