Canonical Allele Identifier:
CA2580593914
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.160668785G>T , CM000668.2:g.160668785G>T | GRCh38 |
| NC_000006.11:g.161089817G>T , CM000668.1:g.161089817G>T | GRCh37 |
| NC_000006.10:g.161009807G>T | NCBI36 |
| NG_016147.1:g.2591C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452651.1:n.115-2412C>A |