Canonical Allele Identifier:
CA1663216663
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.129551821G= , CM000668.2:g.129551821G= | GRCh38 |
| NC_000006.11:g.129872966G= , CM000668.1:g.129872966G= | GRCh37 |
| NC_000006.10:g.129914659G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| XR_001743859.1:n.586+6237C= | |
| XR_001743860.1:n.586+6237C= | |
| XR_001743861.1:n.586+6237C= | |
| XR_001743863.1:n.586+6237C= | |
| XR_002956395.1:n.5509+721C= | |
| XR_942984.1:n.396+721C= | |
| XR_942985.1:n.396+721C= |