Canonical Allele Identifier:
CA1284431812
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.122369205T= , CM000664.2:g.122369205T= | GRCh38 |
| NC_000002.11:g.123126781T= , CM000664.1:g.123126781T= | GRCh37 |
| NC_000002.10:g.122843251T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923278.1:n.556-23758T= | ||
| XR_001739684.1:n.556-23758T= |