Canonical Allele Identifier:
CA1605276900
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.465964T= , CM000668.2:g.465964T= | GRCh38 |
| NC_000006.11:g.465964T= , CM000668.1:g.465964T= | GRCh37 |
| NC_000006.10:g.410964T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_926364.1:n.2714+12239T= | ||
| XR_926365.1:n.2548+12239T= | ||
| XR_001743914.1:n.482-9244T= |