Canonical Allele Identifier:
CA1595022664
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.159333169G= , CM000667.2:g.159333169G= | GRCh38 |
| NC_000005.9:g.158760177G= , CM000667.1:g.158760177G= | GRCh37 |
| NC_000005.8:g.158692755G= | NCBI36 |
| NG_009618.1:g.2305C= , LRG_71:g.2305C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_037889.1:n.745+166G= |