Canonical Allele Identifier:
CA1646022958
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.90708033G= , CM000668.2:g.90708033G= | GRCh38 |
| NC_000006.11:g.91417752G= , CM000668.1:g.91417752G= | GRCh37 |
| NC_000006.10:g.91474473G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001744259.1:n.1243+46531G= |