Canonical Allele Identifier:
CA513685618
Gene:
Linked Data
MyVariant Identifiers:
chr22:g.23915269A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.23573082A>C , CM000684.2:g.23573082A>C | GRCh38 |
| NC_000022.10:g.23915269A>C , CM000684.1:g.23915269A>C | GRCh37 |
| NC_000022.9:g.22245269A>C | NCBI36 |
| NG_009791.1:g.12227T>G , LRG_69:g.12227T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938078.1:n.687A>C | ||
| XR_938078.2:n.1271A>C |