Canonical Allele Identifier:
CA219001071
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.21655796G>T , CM000673.2:g.21655796G>T | GRCh38 |
| NC_000011.9:g.21677342G>T , CM000673.1:g.21677342G>T | GRCh37 |
| NC_000011.8:g.21633918G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001748150.1:n.348-7812C>A |