Canonical Allele Identifier:
CA1649498195
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.98014618G= , CM000668.2:g.98014618G= | GRCh38 |
| NC_000006.11:g.98462494G= , CM000668.1:g.98462494G= | GRCh37 |
| NC_000006.10:g.98569215G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_245563.2:n.371+45152G= | ||
| XR_942809.1:n.371+45152G= |