Canonical Allele Identifier:
CA2838197174
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.156710768G>A , CM000663.2:g.156710768G>A | GRCh38 |
| NC_000001.10:g.156680560G>A , CM000663.1:g.156680560G>A | GRCh37 |
| NC_000001.9:g.154947184G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922176.1:n.1182C>T | ||
| XR_922177.1:n.1073C>T | ||
| XR_922178.1:n.1603C>T | ||
| XR_922179.1:n.1437C>T | ||
| XR_922180.1:n.1104C>T |