Canonical Allele Identifier:
CA1582992062
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.132053814T= , CM000667.2:g.132053814T= | GRCh38 |
| NC_000005.9:g.131389507T= , CM000667.1:g.131389507T= | GRCh37 |
| NC_000005.8:g.131417406T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_948785.1:n.229-210A= | ||
| XR_001742531.1:n.244-210A= | ||
| XR_948785.2:n.252-210A= |