Linked Data
dbSNP Id:
rs4906902
gnomAD v2:
15-27019768-A-G
gnomAD v3:
15-26774621-A-G
gnomAD v4:
15-26774621-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.26774621A>G , CM000677.2:g.26774621A>G | GRCh38 |
| NC_000015.9:g.27019768A>G , CM000677.1:g.27019768A>G | GRCh37 |
| NC_000015.8:g.24570861A>G | NCBI36 |
| NG_012836.1:g.4160T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000541819.6:c.249-1849T>C | ENSP00000442408.2:n.249-1849T>C | |
| ENST00000557641.5:n.453-1849T>C |