Canonical Allele Identifier:
CA2293960288
Gene:
Linked Data
dbSNP Id:
rs2031436434
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31756983T>C , CM000680.2:g.31756983T>C | GRCh38 |
| NC_000018.9:g.29336946T>C , CM000680.1:g.29336946T>C | GRCh37 |
| NC_000018.8:g.27590944T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_935338.1:n.66-5156T>C |