Canonical Allele Identifier:
CA1672979009
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.151633455C= , CM000668.2:g.151633455C= | GRCh38 |
| NC_000006.11:g.151954590C= , CM000668.1:g.151954590C= | GRCh37 |
| NC_000006.10:g.151996283C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_943115.1:n.2496+3473C= |