dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.11494200T>A , CM000680.2:g.11494200T>A | GRCh38 |
| NC_000018.9:g.11494199T>A , CM000680.1:g.11494199T>A | GRCh37 |
| NC_000018.8:g.11484199T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_110778.1:n.194+3959T>A | ||
| NR_110779.1:n.115+5278T>A |