Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.22115028T= , CM000671.2:g.22115028T= | GRCh38 |
| NC_000009.11:g.22115027T= , CM000671.1:g.22115027T= | GRCh37 |
| NC_000009.10:g.22105027T= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_003529.3:n.2908+1229T= | ||
| NR_047532.1:n.1697+1229T= | ||
| NR_047534.1:n.961+1229T= | ||
| NR_047535.1:n.856+2633T= | ||
| NR_047536.1:n.720+2633T= | ||
| NR_047537.1:n.781-5172T= | ||
| NR_047538.1:n.645-5172T= | ||
| NR_047543.1:n.990+1229T= | ||
| NR_120536.1:n.645-5476T= |