Canonical Allele Identifier:
CA1458504922
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.54228599C= , CM000666.2:g.54228599C= | GRCh38 |
| NC_000004.11:g.55094766C= , CM000666.1:g.55094766C= | GRCh37 |
| NC_000004.10:g.54789523C= | NCBI36 |
| NG_009250.1:g.4503C= , LRG_309:g.4503C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000507166.5:c.1018-46326C= | ENSP00000423325.1:n.1018-46326C= |