Canonical Allele Identifier:
CA1350283918
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.21207027A= , CM000665.2:g.21207027A= | GRCh38 |
| NC_000003.11:g.21248519A= , CM000665.1:g.21248519A= | GRCh37 |
| NC_000003.10:g.21223523A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_940646.1:n.254-3971A= | ||
| XR_940646.2:n.547-3971A= |