Canonical Allele Identifier:
CA513685559
Gene:
Linked Data
MyVariant Identifiers:
chr22:g.23915250C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.23573063C>T , CM000684.2:g.23573063C>T | GRCh38 |
| NC_000022.10:g.23915250C>T , CM000684.1:g.23915250C>T | GRCh37 |
| NC_000022.9:g.22245250C>T | NCBI36 |
| NG_009791.1:g.12246G>A , LRG_69:g.12246G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938075.1:n.704C>T | ||
| XR_938076.1:n.769C>T | ||
| XR_938078.1:n.668C>T | ||
| XR_938079.1:n.561C>T | ||
| XR_938075.2:n.1288C>T | ||
| XR_938078.2:n.1252C>T |