Canonical Allele Identifier:
CA1168497118
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.56262196T= , CM000663.2:g.56262196T= | GRCh38 |
| NC_000001.10:g.56727868T= , CM000663.1:g.56727868T= | GRCh37 |
| NC_000001.9:g.56500456T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641109.1:c.760-12996A= | ENSP00000493138.1:n.760-12996A= | |
| ENST00000641346.1:c.367-12996A= | ||
| ENST00000641415.1:c.193-8303A= | ||
| ENST00000641494.1:c.379-12996A= | ||
| ENST00000642129.1:c.769-12996A= |