Canonical Allele Identifier:
CA1940774007
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.120961461C= , CM000672.2:g.120961461C= | GRCh38 |
| NC_000010.10:g.122720974C= , CM000672.1:g.122720974C= | GRCh37 |
| NC_000010.9:g.122710964C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_946372.1:n.99+19191G= | ||
| XR_001747609.1:n.540+19191G= | ||
| XR_946372.2:n.1002+19191G= |