Canonical Allele Identifier:
CA1139985660
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.72285502T= , CM000663.2:g.72285502T= | GRCh38 |
| NC_000001.10:g.72751185T= , CM000663.1:g.72751185T= | GRCh37 |
| NC_000001.9:g.72523773T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_947505.1:n.310+2097T= | ||
| XR_947506.1:n.310+2097T= | ||
| XR_947507.1:n.310+2097T= | ||
| XR_001737670.1:n.414+2097T= | ||
| XR_001737671.2:n.418+2097T= | ||
| XR_947505.2:n.414+2097T= | ||
| XR_947506.2:n.414+2097T= |