Linked Data
dbSNP Id:
rs2041060478
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.80152749G>C , CM000677.2:g.80152749G>C | GRCh38 |
| NC_000015.9:g.80445091G>C , CM000677.1:g.80445091G>C | GRCh37 |
| NC_000015.8:g.78232146G>C | NCBI36 |
| NG_012833.1:g.4751G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000558022.5:c.-30+204G>C | ENSP00000453152.1:n.-30+204G>C |