Canonical Allele Identifier:
CA1464986466
Community Standard Title: NC_000004.12:g.66868139G>C
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.66868139G>C , CM000666.2:g.66868139G>C | GRCh38 |
| NC_000004.11:g.67733857G>C , CM000666.1:g.67733857G>C | GRCh37 |
| NC_000004.10:g.67416452G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_938847.1:n.262C>G | |
| XR_938847.2:n.509C>G | |
| XR_938848.1:n.179+2627C>G | |
| XR_938848.2:n.426+2627C>G |