Canonical Allele Identifier:
CA1328655589
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.218216574T= , CM000664.2:g.218216574T= | GRCh38 |
| NC_000002.11:g.219081297T= , CM000664.1:g.219081297T= | GRCh37 |
| NC_000002.10:g.218789542T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_241416.2:n.371A= | ||
| XR_923908.1:n.368A= |