Canonical Allele Identifier:
CA76548605
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.71785378C>G , CM000665.2:g.71785378C>G | GRCh38 |
| NC_000003.11:g.71834529C>G , CM000665.1:g.71834529C>G | GRCh37 |
| NC_000003.10:g.71917219C>G | NCBI36 |
| NG_008275.1:g.4829G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_940951.1:n.22C>G | ||
| XR_940952.1:n.22C>G | ||
| XR_940953.1:n.22C>G | ||
| XR_940954.1:n.22C>G | ||
| XR_940955.1:n.22C>G | ||
| XR_940956.1:n.48C>G | ||
| XR_001740744.1:n.103C>G | ||
| XR_001740745.1:n.103C>G | ||
| XR_001740746.1:n.103C>G | ||
| XR_001740747.1:n.103C>G | ||
| XR_940951.2:n.103C>G | ||
| XR_940952.2:n.103C>G | ||
| XR_940955.2:n.103C>G |