Canonical Allele Identifier:
CA1816697745
Gene:
Linked Data
dbSNP Id:
rs1814530175
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.123753560T>C , CM000670.2:g.123753560T>C | GRCh38 |
| NC_000008.10:g.124765800T>C , CM000670.1:g.124765800T>C | GRCh37 |
| NC_000008.9:g.124834981T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_928607.1:n.153-11223T>C | ||
| XR_928607.3:n.324-11223T>C |