Canonical Allele Identifier:
CA2584328058
Gene:
Linked Data
gnomAD v4:
19-33521936-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.33521936C>T , CM000681.2:g.33521936C>T | GRCh38 |
| NC_000019.9:g.34012842C>T , CM000681.1:g.34012842C>T | GRCh37 |
| NC_000019.8:g.38704682C>T | NCBI36 |
| NG_013358.1:g.4958G>A | |
| NG_013358.2:g.4958G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_001754035.2:n.3C>T | ||
| XR_935918.2:n.3C>T |