Canonical Allele Identifier:
CA1161925203
Gene:
Linked Data
dbSNP Id:
rs1023779902
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.34523551C>A , CM000663.2:g.34523551C>A | GRCh38 |
| NC_000001.10:g.34989152C>A , CM000663.1:g.34989152C>A | GRCh37 |
| NC_000001.9:g.34761739C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_947171.1:n.1073+24028G>T | ||
| XR_001737964.1:n.991+24028G>T |