Canonical Allele Identifier:
CA1500737980
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.144559692A= , CM000666.2:g.144559692A= | GRCh38 |
| NC_000004.11:g.145480844A= , CM000666.1:g.145480844A= | GRCh37 |
| NC_000004.10:g.145700294A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000649263.1:c.328-143714T= | ENSP00000497507.1:n.328-143714T= | |
| XR_939272.1:n.178+2292T= | ||
| XR_939273.1:n.178+2292T= | ||
| XR_939272.2:n.522+2292T= | ||
| XR_939273.2:n.522+2292T= |