Canonical Allele Identifier:
CA2637311333
Gene:
Linked Data
gnomAD v4:
17-35880800-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.35880800G>T , CM000679.2:g.35880800G>T | GRCh38 |
| NC_000017.9:g.31231917G>T | NCBI36 |
| NG_015990.1:g.4574C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_934696.1:n.197-3582G>T | ||
| XR_934697.1:n.200-3582G>T | ||
| XR_001752852.1:n.426+726G>T | ||
| XR_934696.2:n.91-3582G>T | ||
| XR_934697.2:n.91-3582G>T |