Canonical Allele Identifier:
CA11468745
Community Standard Title: NC_000003.12:g.21207150C>T
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.21207150C>T , CM000665.2:g.21207150C>T | GRCh38 |
| NC_000003.11:g.21248642C>T , CM000665.1:g.21248642C>T | GRCh37 |
| NC_000003.10:g.21223646C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_940646.1:n.254-3848C>T | |
| XR_940646.2:n.547-3848C>T |