Canonical Allele Identifier:
CA2047473650
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.76615280A= , CM000674.2:g.76615280A= | GRCh38 |
| NC_000012.11:g.77009060A= , CM000674.1:g.77009060A= | GRCh37 |
| NC_000012.10:g.75533191A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_945113.1:n.513-23A= | ||
| XR_001749220.1:n.477-23A= | ||
| XR_945113.3:n.532-23A= |