Canonical Allele Identifier:
CA1649498176
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.98014590T= , CM000668.2:g.98014590T= | GRCh38 |
| NC_000006.11:g.98462466T= , CM000668.1:g.98462466T= | GRCh37 |
| NC_000006.10:g.98569187T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_245563.2:n.371+45124T= | ||
| XR_942809.1:n.371+45124T= |