Canonical Allele Identifier:
CA1100909317
Gene:
Linked Data
dbSNP Id:
rs1784762162
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.46032903G>A , CM000669.2:g.46032903G>A | GRCh38 |
| NC_000007.13:g.46072501G>A , CM000669.1:g.46072501G>A | GRCh37 |
| NC_000007.12:g.46039026G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001745203.1:n.1270-3715G>A |