Canonical Allele Identifier:
CA2293960172
Gene:
Linked Data
dbSNP Id:
rs2031433548
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31756734C>T , CM000680.2:g.31756734C>T | GRCh38 |
| NC_000018.9:g.29336697C>T , CM000680.1:g.29336697C>T | GRCh37 |
| NC_000018.8:g.27590695C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_935338.1:n.66-5405C>T |