Canonical Allele Identifier:
CA1283590565
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.120548864G= , CM000664.2:g.120548864G= | GRCh38 |
| NC_000002.11:g.121306440G= , CM000664.1:g.121306440G= | GRCh37 |
| NC_000002.10:g.121022910G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_923262.1:n.1488-1527C= | ||
| XR_001739680.2:n.1496-1527C= | ||
| XR_001739681.2:n.2129-2105C= | ||
| XR_001739682.1:n.1496-2105C= | ||
| XR_002959417.1:n.1496-2105C= |