Canonical Allele Identifier:
CA1608913798
Gene:
Linked Data
dbSNP Id:
rs994845217
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.8169573C>T , CM000668.2:g.8169573C>T | GRCh38 |
| NC_000006.11:g.8169806C>T , CM000668.1:g.8169806C>T | GRCh37 |
| NC_000006.10:g.8114805C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_926440.1:n.82+11313C>T | ||
| XR_926441.1:n.189+1653C>T | ||
| XR_926442.1:n.82+11313C>T | ||
| XR_926443.1:n.82+11313C>T | ||
| XR_001743950.1:n.179+1653C>T | ||
| XR_926440.2:n.74+11313C>T | ||
| XR_926441.2:n.179+1653C>T | ||
| XR_926443.2:n.83+11313C>T |