Canonical Allele Identifier:
CA1704517815
Gene:
Linked Data
dbSNP Id:
rs1784763636
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.46033030T>A , CM000669.2:g.46033030T>A | GRCh38 |
| NC_000007.13:g.46072628T>A , CM000669.1:g.46072628T>A | GRCh37 |
| NC_000007.12:g.46039153T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001745203.1:n.1270-3588T>A |