Canonical Allele Identifier:
CA513685649
Gene:
Linked Data
MyVariant Identifiers:
chr22:g.23915280T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.23573093T>A , CM000684.2:g.23573093T>A | GRCh38 |
| NC_000022.10:g.23915280T>A , CM000684.1:g.23915280T>A | GRCh37 |
| NC_000022.9:g.22245280T>A | NCBI36 |
| NG_009791.1:g.12216A>T , LRG_69:g.12216A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938078.1:n.698T>A | ||
| XR_938078.2:n.1282T>A |