Canonical Allele Identifier:
CA1140445732
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.153023685G= , CM000663.2:g.153023685G= | GRCh38 |
| NC_000001.10:g.152996161G= , CM000663.1:g.152996161G= | GRCh37 |
| NC_000001.9:g.151262785G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_922151.1:n.101-258G= | |
| XR_922152.1:n.191-258G= |