Canonical Allele Identifier:
CA154151486
Gene:
Linked Data
dbSNP Id:
rs10178082
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.10667285T>A , CM000669.2:g.10667285T>A | GRCh38 |
| NC_000007.13:g.10706912T>A , CM000669.1:g.10706912T>A | GRCh37 |
| NC_000007.12:g.10673437T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_147499.1:n.64-105708A>T | ||
| XR_001745090.1:n.376-8011T>A |