Canonical Allele Identifier:
CA1161925187
Gene:
Linked Data
dbSNP Id:
rs1639362609
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.34523508T>C , CM000663.2:g.34523508T>C | GRCh38 |
| NC_000001.10:g.34989109T>C , CM000663.1:g.34989109T>C | GRCh37 |
| NC_000001.9:g.34761696T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_947171.1:n.1073+24071A>G | ||
| XR_001737964.1:n.991+24071A>G |