Canonical Allele Identifier:
CA189070553
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.7925381T>G , CM000671.2:g.7925381T>G | GRCh38 |
| NC_000009.11:g.7925381T>G , CM000671.1:g.7925381T>G | GRCh37 |
| NC_000009.10:g.7915381T>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_929462.1:n.664+164A>C | ||
| XR_929463.1:n.664+164A>C | ||
| XR_929462.2:n.664+164A>C | ||
| XR_929463.2:n.664+164A>C |