Canonical Allele Identifier:
CA1500739008
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.144601375C= , CM000666.2:g.144601375C= | GRCh38 |
| NC_000004.11:g.145522527C= , CM000666.1:g.145522527C= | GRCh37 |
| NC_000004.10:g.145741977C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649263.1:c.328-185397G= | ENSP00000497507.1:n.328-185397G= |