Canonical Allele Identifier:
CA513685616
Gene:
Linked Data
MyVariant Identifiers:
chr22:g.23915268C>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.23573081C>G , CM000684.2:g.23573081C>G | GRCh38 |
| NC_000022.10:g.23915268C>G , CM000684.1:g.23915268C>G | GRCh37 |
| NC_000022.9:g.22245268C>G | NCBI36 |
| NG_009791.1:g.12228G>C , LRG_69:g.12228G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938078.1:n.686C>G | ||
| XR_938078.2:n.1270C>G |