dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.130910288A>C , CM000669.2:g.130910288A>C | GRCh38 |
| NC_000007.13:g.130595047A>C , CM000669.1:g.130595047A>C | GRCh37 |
| NC_000007.12:g.130245587A>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_034120.1:n.403+1822T>G | ||
| NR_110472.1:n.403+1822T>G | ||
| NR_110473.1:n.403+1822T>G | ||
| NR_170175.1:n.1765+1822T>G | ||
| NR_170176.1:n.1599-25892T>G |