Canonical Allele Identifier:
CA1427674238
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.187999098A= , CM000665.2:g.187999098A= | GRCh38 |
| NC_000003.11:g.187716886A= , CM000665.1:g.187716886A= | GRCh37 |
| NC_000003.10:g.189199580A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001741061.1:n.416-1340T= | ||
| XR_001741062.1:n.295-1340T= |