Canonical Allele Identifier:
CA2129379125
Gene:
Linked Data
dbSNP Id:
rs1882064415
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.36385051T>C , CM000676.2:g.36385051T>C | GRCh38 |
| NC_000014.8:g.36854256T>C , CM000676.1:g.36854256T>C | GRCh37 |
| NC_000014.7:g.35924007T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011537428.1:c.319-12108T>C | XP_011535730.1:n.319-12108T>C | |
| XR_943756.1:n.358+23955T>C |