Canonical Allele Identifier:
CA1769199529
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.20130192C= , CM000670.2:g.20130192C= | GRCh38 |
| NC_000008.10:g.19987703C= , CM000670.1:g.19987703C= | GRCh37 |
| NC_000008.9:g.20031983C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_949563.1:n.3408+273C= | |
| XR_949563.2:n.3400+273C= |