Linked Data
dbSNP Id:
rs539194398
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.46897283G>A , CM000675.2:g.46897283G>A | GRCh38 |
| NC_000013.10:g.47471418G>A , CM000675.1:g.47471418G>A | GRCh37 |
| NC_000013.9:g.46369419G>A | NCBI36 |
| NG_013011.1:g.4752C>T |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NM_001378924.1:c.-329+669C>T | NP_001365853.1:n.-329+669C>T |