Canonical Allele Identifier:
CA2493232078
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.20485675C= , CM000664.2:g.20485675C= | GRCh38 |
| NC_000002.11:g.20685436C= , CM000664.1:g.20685436C= | GRCh37 |
| NC_000002.10:g.20548917C= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_157978.1:n.530+3063G= |