Canonical Allele Identifier:
CA1649534262
Gene:
Linked Data
dbSNP Id:
rs1468441605
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.98102475C>T , CM000668.2:g.98102475C>T | GRCh38 |
| NC_000006.11:g.98550351C>T , CM000668.1:g.98550351C>T | GRCh37 |
| NC_000006.10:g.98657072C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_245563.2:n.456+3205C>T | ||
| XR_942809.1:n.456+3205C>T |