Canonical Allele Identifier:
CA513685599
Gene:
Linked Data
MyVariant Identifiers:
chr22:g.23915263A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.23573076A>T , CM000684.2:g.23573076A>T | GRCh38 |
| NC_000022.10:g.23915263A>T , CM000684.1:g.23915263A>T | GRCh37 |
| NC_000022.9:g.22245263A>T | NCBI36 |
| NG_009791.1:g.12233T>A , LRG_69:g.12233T>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938078.1:n.681A>T | ||
| XR_938078.2:n.1265A>T |