Canonical Allele Identifier:
CA1267947484
Gene:
Linked Data
dbSNP Id:
rs553772116
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.88016279G>A , CM000664.2:g.88016279G>A | GRCh38 |
| NC_000002.11:g.88315798G>A , CM000664.1:g.88315798G>A | GRCh37 |
| NC_000002.10:g.88096913G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_940335.3:n.624G>A | ||
| XR_940336.3:n.624G>A |