Canonical Allele Identifier:
CA1695966116
Gene:
Linked Data
dbSNP Id:
rs1785079762
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.26605832G>A , CM000669.2:g.26605832G>A | GRCh38 |
| NC_000007.13:g.26645451G>A , CM000669.1:g.26645451G>A | GRCh37 |
| NC_000007.12:g.26611976G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_927131.1:n.1118-6462C>T | ||
| XR_927131.2:n.1186-6462C>T |