Canonical Allele Identifier:
CA2839326004
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.66510589C>T , CM000673.2:g.66510589C>T | GRCh38 |
| NC_000011.9:g.66278060C>T , CM000673.1:g.66278060C>T | GRCh37 |
| NC_000011.8:g.66034636C>T | NCBI36 |
| NG_009093.1:g.4942C>T | |
| NG_032068.1:g.35181C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000419755.3:c.159-424C>T | ENSP00000398526.3:n.159-424C>T |