Canonical Allele Identifier:
CA1144697634
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193121830C= , CM000663.2:g.193121830C= | GRCh38 |
| NC_000001.10:g.193090960C= , CM000663.1:g.193090960C= | GRCh37 |
| NC_000001.9:g.191357583C= | NCBI36 |
| NG_012691.1:g.4873C= , LRG_507:g.4873C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001738350.1:n.1827G= |