Canonical Allele Identifier:
CA513685583
Gene:
Linked Data
dbSNP Id:
rs1602286200
gnomAD v4:
22-23573070-C-A
MyVariant Identifiers:
chr22:g.23915257C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.23573070C>A , CM000684.2:g.23573070C>A | GRCh38 |
| NC_000022.10:g.23915257C>A , CM000684.1:g.23915257C>A | GRCh37 |
| NC_000022.9:g.22245257C>A | NCBI36 |
| NG_009791.1:g.12239G>T , LRG_69:g.12239G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| XR_938075.1:n.711C>A | ||
| XR_938076.1:n.776C>A | ||
| XR_938078.1:n.675C>A | ||
| XR_938079.1:n.568C>A | ||
| XR_938075.2:n.1295C>A | ||
| XR_938078.2:n.1259C>A |