Canonical Allele Identifier:
CA1672990485
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151653287C= , CM000668.2:g.151653287C= | GRCh38 |
| NC_000006.11:g.151974422C= , CM000668.1:g.151974422C= | GRCh37 |
| NC_000006.10:g.152016115C= | NCBI36 |
| NG_008493.2:g.1597C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_943115.1:n.2596+1491C= |