Canonical Allele Identifier:
CA2378341195
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.15432901T= , CM000683.2:g.15432901T= | GRCh38 |
| NC_000021.8:g.16805220T= , CM000683.1:g.16805220T= | GRCh37 |
| NC_000021.7:g.15727091T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001754965.2:n.468+11123A= | |
| XR_001754970.2:n.468+11123A= | |
| XR_001754971.2:n.468+11123A= | |
| XR_937593.1:n.552+8325A= |