Canonical Allele Identifier:
CA1610684731
Gene:
Linked Data
dbSNP Id:
rs1581439081
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.11943363C>A , CM000668.2:g.11943363C>A | GRCh38 |
| NC_000006.11:g.11943596C>A , CM000668.1:g.11943596C>A | GRCh37 |
| NC_000006.10:g.12051582C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001743976.1:n.348-8172C>A |