Canonical Allele Identifier:
CA1205766032
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.168649452T= , CM000663.2:g.168649452T= | GRCh38 |
| NC_000001.10:g.168618690T= , CM000663.1:g.168618690T= | GRCh37 |
| NC_000001.9:g.166885314T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922259.1:n.201-8177A= | ||
| XR_922259.2:n.332-8177A= |