Canonical Allele Identifier:
CA1659692041
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.121837124G= , CM000668.2:g.121837124G= | GRCh38 |
| NC_000006.11:g.122158270G= , CM000668.1:g.122158270G= | GRCh37 |
| NC_000006.10:g.122199969G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_942936.1:n.241-20787G= | |
| XR_942936.2:n.241-20787G= | |
| XR_942937.1:n.240+69509G= | |
| XR_942937.3:n.240+69509G= | |
| XR_942938.1:n.241-20787G= | |
| XR_942939.1:n.241-20787G= | |
| XR_942940.1:n.241-20787G= | |
| XR_942941.1:n.241-20787G= |