Linked Data
dbSNP Id:
rs1951112413
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.46897290G>A , CM000675.2:g.46897290G>A | GRCh38 |
| NC_000013.10:g.47471425G>A , CM000675.1:g.47471425G>A | GRCh37 |
| NC_000013.9:g.46369426G>A | NCBI36 |
| NG_013011.1:g.4745C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NM_001378924.1:c.-329+662C>T | NP_001365853.1:n.-329+662C>T |