Canonical Allele Identifier:
CA1139894017
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171122735A= , CM000663.2:g.171122735A= | GRCh38 |
| NC_000001.10:g.171091875A= , CM000663.1:g.171091875A= | GRCh37 |
| NC_000001.9:g.169358499A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_922278.1:n.593-872T= | ||
| XR_001738291.2:n.1392-872T= | ||
| XR_922278.3:n.1392-872T= |