Canonical Allele Identifier:
CA1674885892
Gene:
Linked Data
dbSNP Id:
rs1187265557
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155812652C>T , CM000668.2:g.155812652C>T | GRCh38 |
| NC_000006.11:g.156133786C>T , CM000668.1:g.156133786C>T | GRCh37 |
| NC_000006.10:g.156175478C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943142.1:n.79+19233C>T | ||
| XR_943146.1:n.645-613G>A | ||
| XR_001744423.1:n.699-613G>A | ||
| XR_001744424.1:n.79+19233C>T |