Canonical Allele Identifier:
CA1146624667
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.193121934G= , CM000663.2:g.193121934G= | GRCh38 |
| NC_000001.10:g.193091064G= , CM000663.1:g.193091064G= | GRCh37 |
| NC_000001.9:g.191357687G= | NCBI36 |
| NG_012691.1:g.4977G= , LRG_507:g.4977G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001738350.1:n.1723C= |