Canonical Allele Identifier:
CA11001663
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.15786044T>C , CM000664.2:g.15786044T>C | GRCh38 |
| NC_000002.11:g.15926168T>C , CM000664.1:g.15926168T>C | GRCh37 |
| NC_000002.10:g.15843619T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922821.1:n.1060T>C | ||
| XR_922822.1:n.1039T>C | ||
| XR_922823.1:n.1632T>C |