Canonical Allele Identifier:
CA1800979830
Gene:
Linked Data
dbSNP Id:
rs1808585387
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.88981159T>A , CM000670.2:g.88981159T>A | GRCh38 |
| NC_000008.10:g.89993388T>A , CM000670.1:g.89993388T>A | GRCh37 |
| NC_000008.9:g.90062504T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_002956667.1:n.179-99098A>T |