Canonical Allele Identifier:
CA1649498137
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.98014535A= , CM000668.2:g.98014535A= | GRCh38 |
| NC_000006.11:g.98462411A= , CM000668.1:g.98462411A= | GRCh37 |
| NC_000006.10:g.98569132A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_245563.2:n.371+45069A= | ||
| XR_942809.1:n.371+45069A= |