Canonical Allele Identifier:
CA1250829322
Gene:
Linked Data
dbSNP Id:
rs1668654873
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.52722351G>A , CM000664.2:g.52722351G>A | GRCh38 |
| NC_000002.11:g.52949489G>A , CM000664.1:g.52949489G>A | GRCh37 |
| NC_000002.10:g.52802993G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_002959384.1:n.906C>T |