Canonical Allele Identifier:
CA1143812609
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.56262257G= , CM000663.2:g.56262257G= | GRCh38 |
| NC_000001.10:g.56727929G= , CM000663.1:g.56727929G= | GRCh37 |
| NC_000001.9:g.56500517G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641109.1:c.760-13057C= | ENSP00000493138.1:n.760-13057C= | |
| ENST00000641346.1:c.367-13057C= | ||
| ENST00000641415.1:c.193-8364C= | ||
| ENST00000641494.1:c.379-13057C= | ||
| ENST00000642129.1:c.769-13057C= |