Linked Data
MyVariant Identifiers:
chr9:g.22114962A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.22114963A>G , CM000671.2:g.22114963A>G | GRCh38 |
| NC_000009.11:g.22114962A>G , CM000671.1:g.22114962A>G | GRCh37 |
| NC_000009.10:g.22104962A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_003529.3:n.2908+1164A>G | ||
| NR_047532.1:n.1697+1164A>G | ||
| NR_047534.1:n.961+1164A>G | ||
| NR_047535.1:n.856+2568A>G | ||
| NR_047536.1:n.720+2568A>G | ||
| NR_047537.1:n.781-5237A>G | ||
| NR_047538.1:n.645-5237A>G | ||
| NR_047543.1:n.990+1164A>G | ||
| NR_120536.1:n.645-5541A>G |