Canonical Allele Identifier:
CA1139966421
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.192567683C= , CM000663.2:g.192567683C= | GRCh38 |
| NC_000001.10:g.192536813C= , CM000663.1:g.192536813C= | GRCh37 |
| NC_000001.9:g.190803436C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922382.1:n.267-467G= | ||
| XR_002958418.1:n.288-467G= |