Canonical Allele Identifier:
CA14890235
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.25454202T>C , CM000683.2:g.25454202T>C | GRCh38 |
| NC_000021.8:g.26826514T>C , CM000683.1:g.26826514T>C | GRCh37 |
| NC_000021.7:g.25748385T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_937615.1:n.78-776A>G |