Canonical Allele Identifier:
CA12096867
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.28549074T>C , CM000667.2:g.28549074T>C | GRCh38 |
| NC_000005.9:g.28549181T>C , CM000667.1:g.28549181T>C | GRCh37 |
| NC_000005.8:g.28584938T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001742619.1:n.296-574A>G | |
| XR_001742620.1:n.365-574A>G | |
| XR_925882.1:n.342-574A>G |