Canonical Allele Identifier:
CA1182086474
Gene:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.95680412A>T , CM000663.2:g.95680412A>T | GRCh38 |
| NC_000001.10:g.96145968A>T , CM000663.1:g.96145968A>T | GRCh37 |
| NC_000001.9:g.95918556A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_246378.3:n.116+54847A>T | ||
| XR_947613.1:n.116+54847A>T | ||
| XR_947614.1:n.478+44203A>T | ||
| XR_001738162.2:n.133+54847A>T | ||
| XR_246378.5:n.133+54847A>T |