Canonical Allele Identifier:
CA1695966131
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.26605858G= , CM000669.2:g.26605858G= | GRCh38 |
| NC_000007.13:g.26645477G= , CM000669.1:g.26645477G= | GRCh37 |
| NC_000007.12:g.26612002G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_927131.1:n.1118-6488C= | ||
| XR_927131.2:n.1186-6488C= |