Canonical Allele Identifier:
CA2704846814
Gene:
Linked Data
dbSNP Id:
rs2108529052
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.187931693G>T , CM000665.2:g.187931693G>T | GRCh38 |
| NC_000003.11:g.187649481G>T , CM000665.1:g.187649481G>T | GRCh37 |
| NC_000003.10:g.189132175G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_924814.1:n.1221C>A |