Canonical Allele Identifier:
CA1695966062
Gene:
Linked Data
dbSNP Id:
rs1785078367
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.26605722T>C , CM000669.2:g.26605722T>C | GRCh38 |
| NC_000007.13:g.26645341T>C , CM000669.1:g.26645341T>C | GRCh37 |
| NC_000007.12:g.26611866T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_927131.1:n.1118-6352A>G | ||
| XR_927131.2:n.1186-6352A>G |