Canonical Allele Identifier:
CA1674935819
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.155913388A>T , CM000668.2:g.155913388A>T | GRCh38 |
| NC_000006.11:g.156234522A>T , CM000668.1:g.156234522A>T | GRCh37 |
| NC_000006.10:g.156276214A>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943142.1:n.669-1423A>T | ||
| XR_943143.1:n.1169-1423A>T | ||
| XR_943144.1:n.530-1423A>T | ||
| XR_943146.1:n.352-80494T>A | ||
| XR_001744423.1:n.406-80494T>A |