Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.22114573T= , CM000671.2:g.22114573T= | GRCh38 |
| NC_000009.11:g.22114572T= , CM000671.1:g.22114572T= | GRCh37 |
| NC_000009.10:g.22104572T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_003529.3:n.2908+774T= | ||
| NR_047532.1:n.1697+774T= | ||
| NR_047534.1:n.961+774T= | ||
| NR_047535.1:n.856+2178T= | ||
| NR_047536.1:n.720+2178T= | ||
| NR_047537.1:n.781-5627T= | ||
| NR_047538.1:n.645-5627T= | ||
| NR_047543.1:n.990+774T= | ||
| NR_120536.1:n.645-5931T= |