Canonical Allele Identifier:
CA1284431732
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.122369062T= , CM000664.2:g.122369062T= | GRCh38 |
| NC_000002.11:g.123126638T= , CM000664.1:g.123126638T= | GRCh37 |
| NC_000002.10:g.122843108T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923278.1:n.556-23901T= | ||
| XR_001739684.1:n.556-23901T= |