Canonical Allele Identifier:
CA1929213471
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94762614T= , CM000672.2:g.94762614T= | GRCh38 |
| NC_000010.10:g.96522371T= , CM000672.1:g.96522371T= | GRCh37 |
| NC_000010.9:g.96512361T= | NCBI36 |
| NG_008384.2:g.4909T= | |
| NG_008384.3:g.4934T= |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000464755.1:c.932-12444T= | ENSP00000483243.1:n.932-12444T= |