dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.118996132T>A , CM000670.2:g.118996132T>A | GRCh38 |
| NC_000008.10:g.120008371T>A , CM000670.1:g.120008371T>A | GRCh37 |
| NC_000008.9:g.120077552T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000521788.1:n.122+559T>A | ||
| XM_005250756.2:c.-60+43754T>A | XP_005250813.1:n.-60+43754T>A | |
| NM_001324095.1:c.-323-41304T>A | NP_001311024.1:n.-323-41304T>A | |
| XM_005250756.3:c.-60+43754T>A | XP_005250813.1:n.-60+43754T>A | |
| NM_001324095.2:c.-323-41304T>A | NP_001311024.1:n.-323-41304T>A |