Linked Data
MyVariant Identifiers:
chr22:g.22012572T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.21658283T>A , CM000684.2:g.21658283T>A | GRCh38 |
| NC_000022.10:g.22012572T>A , CM000684.1:g.22012572T>A | GRCh37 |
| NC_000022.9:g.20342572T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000641967.1:n.180T>A | ||
| ENST00000498589.1:n.360T>A | ||
| XM_017029165.1:c.495T>A | XP_016884654.1:p.Val165= | |
| NR_169729.1:n.1095T>A | ||
| NR_169730.1:n.998T>A | ||
| NR_169731.1:n.432-2554T>A | ||
| NR_169732.1:n.149T>A | ||
| NR_169733.1:n.214-7T>A | ||
| NR_169734.1:n.231T>A |