Canonical Allele Identifier:
CA1282456492
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.118079775T= , CM000664.2:g.118079775T= | GRCh38 |
| NC_000002.11:g.118837351T= , CM000664.1:g.118837351T= | GRCh37 |
| NC_000002.10:g.118553821T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XM_011512305.1:c.697-2243A= | XP_011510607.1:n.697-2243A= | |
| XR_001739662.2:n.138+8476A= |