Canonical Allele Identifier:
CA1649498191
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.98014615A= , CM000668.2:g.98014615A= | GRCh38 |
| NC_000006.11:g.98462491A= , CM000668.1:g.98462491A= | GRCh37 |
| NC_000006.10:g.98569212A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_245563.2:n.371+45149A= | ||
| XR_942809.1:n.371+45149A= |