Canonical Allele Identifier:
CA1361840248
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.45818159G= , CM000665.2:g.45818159G= | GRCh38 |
| NC_000003.11:g.45859651G= , CM000665.1:g.45859651G= | GRCh37 |
| NC_000003.10:g.45834655G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001740681.1:n.781G= |