Canonical Allele Identifier:
CA2710457449
Gene:
Linked Data
dbSNP Id:
rs1580994515
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.162656582G>T , CM000667.2:g.162656582G>T | GRCh38 |
| NC_000005.9:g.162083588G>T , CM000667.1:g.162083588G>T | GRCh37 |
| NC_000005.8:g.162016166G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001742958.1:n.418+3520C>A |