Canonical Allele Identifier:
CA2580585669
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.41534660C>G , CM000664.2:g.41534660C>G | GRCh38 |
| NC_000002.11:g.41761800C>G , CM000664.1:g.41761800C>G | GRCh37 |
| NC_000002.10:g.41615304C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_939996.1:n.181+3066G>C | ||
| XR_939997.1:n.146+3066G>C | ||
| XR_939997.2:n.9529+3066G>C |