Canonical Allele Identifier:
CA1649498092
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.98014476G= , CM000668.2:g.98014476G= | GRCh38 |
| NC_000006.11:g.98462352G= , CM000668.1:g.98462352G= | GRCh37 |
| NC_000006.10:g.98569073G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_245563.2:n.371+45010G= | ||
| XR_942809.1:n.371+45010G= |