Canonical Allele Identifier:
CA2255112042
Gene:
Linked Data
dbSNP Id:
rs1907327780
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.30237349G>A , CM000679.2:g.30237349G>A | GRCh38 |
| NC_000017.10:g.28564367G>A , CM000679.1:g.28564367G>A | GRCh37 |
| NC_000017.9:g.25588493G>A | NCBI36 |
| NG_011747.2:g.3588C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_934654.1:n.165+279G>A | ||
| XR_001752824.1:n.280+279G>A |