Canonical Allele Identifier:
CA1674885746
Gene:
Linked Data
dbSNP Id:
rs1322347114
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155812495C>G , CM000668.2:g.155812495C>G | GRCh38 |
| NC_000006.11:g.156133629C>G , CM000668.1:g.156133629C>G | GRCh37 |
| NC_000006.10:g.156175321C>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943142.1:n.79+19076C>G | ||
| XR_943146.1:n.645-456G>C | ||
| XR_001744423.1:n.699-456G>C | ||
| XR_001744424.1:n.79+19076C>G |