Canonical Allele Identifier:
CA2566573022
Gene:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.2818661G>A , CM000686.2:g.2818661G>A | GRCh38 |
| NC_000024.9:g.2686702G>A , CM000686.1:g.2686702G>A | GRCh37 |
| NC_000024.8:g.2746702G>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000679518.1:n.107-22825G>A | ||
| ENST00000681787.1:n.107-22367G>A | ||
| ENST00000681940.1:n.107-26985G>A |