Canonical Allele Identifier:
CA1898741333
Gene:
Linked Data
dbSNP Id:
rs10826566
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.29075768G>C , CM000672.2:g.29075768G>C | GRCh38 |
| NC_000010.10:g.29364697G>C , CM000672.1:g.29364697G>C | GRCh37 |
| NC_000010.9:g.29404703G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_001747284.1:n.127-3724G>C |