Canonical Allele Identifier:
CA1674885858
Gene:
Linked Data
dbSNP Id:
rs1778858255
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155812616A>G , CM000668.2:g.155812616A>G | GRCh38 |
| NC_000006.11:g.156133750A>G , CM000668.1:g.156133750A>G | GRCh37 |
| NC_000006.10:g.156175442A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943142.1:n.79+19197A>G | ||
| XR_943146.1:n.645-577T>C | ||
| XR_001744423.1:n.699-577T>C | ||
| XR_001744424.1:n.79+19197A>G |