Canonical Allele Identifier:
CA566350496
Community Standard Title: NC_000006.12:g.31559979G>C
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31559979G>C , CM000668.2:g.31559979G>C | GRCh38 |
| NC_000006.11:g.31527756G>C , CM000668.1:g.31527756G>C | GRCh37 |
| NC_000006.10:g.31635735G>C | NCBI36 |
| NG_012344.1:g.18129G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NR_149045.1:n.865C>G | |
| XR_926695.1:n.117-9420C>G |