Canonical Allele Identifier:
CA513685572
Gene:
Linked Data
MyVariant Identifiers:
chr22:g.23915253A>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.23573066A>C , CM000684.2:g.23573066A>C | GRCh38 |
| NC_000022.10:g.23915253A>C , CM000684.1:g.23915253A>C | GRCh37 |
| NC_000022.9:g.22245253A>C | NCBI36 |
| NG_009791.1:g.12243T>G , LRG_69:g.12243T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938075.1:n.707A>C | ||
| XR_938076.1:n.772A>C | ||
| XR_938078.1:n.671A>C | ||
| XR_938079.1:n.564A>C | ||
| XR_938075.2:n.1291A>C | ||
| XR_938078.2:n.1255A>C |