Canonical Allele Identifier:
CA1723810365
Gene:
Linked Data
dbSNP Id:
rs536354831
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.87913758C>T , CM000669.2:g.87913758C>T | GRCh38 |
| NC_000007.13:g.87543073C>T , CM000669.1:g.87543073C>T | GRCh37 |
| NC_000007.12:g.87381009C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_927723.1:n.148+143G>A | ||
| XR_927724.1:n.192+143G>A |