Canonical Allele Identifier:
CA1216113171
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193121839C= , CM000663.2:g.193121839C= | GRCh38 |
| NC_000001.10:g.193090969C= , CM000663.1:g.193090969C= | GRCh37 |
| NC_000001.9:g.191357592C= | NCBI36 |
| NG_012691.1:g.4882C= , LRG_507:g.4882C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001738350.1:n.1818G= |