Canonical Allele Identifier:
CA1500739422
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.144601569A= , CM000666.2:g.144601569A= | GRCh38 |
| NC_000004.11:g.145522721A= , CM000666.1:g.145522721A= | GRCh37 |
| NC_000004.10:g.145742171A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649263.1:c.328-185591T= | ENSP00000497507.1:n.328-185591T= |