Canonical Allele Identifier:
CA1895825828
Gene:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.21744013A>T , CM000672.2:g.21744013A>T | GRCh38 |
| NC_000010.10:g.22032942A>T , CM000672.1:g.22032942A>T | GRCh37 |
| NC_000010.9:g.22072948A>T | NCBI36 |
| NG_027818.1:g.214842A>T | |
| NG_027818.2:g.214842A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001747388.1:n.1010+6427T>A |