Canonical Allele Identifier:
CA1674885680
Gene:
Linked Data
dbSNP Id:
rs1778855918
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155812440T>C , CM000668.2:g.155812440T>C | GRCh38 |
| NC_000006.11:g.156133574T>C , CM000668.1:g.156133574T>C | GRCh37 |
| NC_000006.10:g.156175266T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943142.1:n.79+19021T>C | ||
| XR_943146.1:n.645-401A>G | ||
| XR_001744423.1:n.699-401A>G | ||
| XR_001744424.1:n.79+19021T>C |