Canonical Allele Identifier:
CA337532922
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.21312462T>A , CM000686.2:g.21312462T>A | GRCh38 |
| NC_000024.9:g.23474348T>A , CM000686.1:g.23474348T>A | GRCh37 |
| NC_000024.8:g.21883736T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000437359.1:n.288+462T>A |