Canonical Allele Identifier:
CA513685621
Gene:
Linked Data
MyVariant Identifiers:
chr22:g.23915270T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.23573083T>G , CM000684.2:g.23573083T>G | GRCh38 |
| NC_000022.10:g.23915270T>G , CM000684.1:g.23915270T>G | GRCh37 |
| NC_000022.9:g.22245270T>G | NCBI36 |
| NG_009791.1:g.12226A>C , LRG_69:g.12226A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938078.1:n.688T>G | ||
| XR_938078.2:n.1272T>G |