Canonical Allele Identifier:
CA1374121558
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.72266787T= , CM000665.2:g.72266787T= | GRCh38 |
| NC_000003.11:g.72315938T= , CM000665.1:g.72315938T= | GRCh37 |
| NC_000003.10:g.72398628T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_940958.1:n.835+8321A= |