Canonical Allele Identifier:
CA1695966065
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.26605731T= , CM000669.2:g.26605731T= | GRCh38 |
| NC_000007.13:g.26645350T= , CM000669.1:g.26645350T= | GRCh37 |
| NC_000007.12:g.26611875T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_927131.1:n.1118-6361A= | ||
| XR_927131.2:n.1186-6361A= |