Canonical Allele Identifier:
CA1416869621
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.164044176A= , CM000665.2:g.164044176A= | GRCh38 |
| NC_000003.11:g.163761964A= , CM000665.1:g.163761964A= | GRCh37 |
| NC_000003.10:g.165244658A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001740997.1:n.472-13480T= | ||
| XR_427434.3:n.296-13480T= |