Linked Data
dbSNP Id:
rs10468017
gnomAD v2:
15-58678512-C-T
gnomAD v3:
15-58386313-C-T
gnomAD v4:
15-58386313-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.58386313C>T , CM000677.2:g.58386313C>T | GRCh38 |
| NC_000015.9:g.58678512C>T , CM000677.1:g.58678512C>T | GRCh37 |
| NC_000015.8:g.56465804C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000558239.5:c.-172+33658G>A | ENSP00000453292.1:n.-172+33658G>A | |
| ENST00000560863.5:n.415+33658G>A | ||
| XR_429537.2:n.164+33658G>A | ||
| XR_932289.1:n.165-1457G>A | ||
| XR_001751556.2:n.216+33658G>A | ||
| XR_001751557.2:n.216+33658G>A | ||
| XR_001751558.2:n.216+33658G>A | ||
| XR_001751559.2:n.216+33658G>A | ||
| XR_001751560.2:n.216+33658G>A | ||
| XR_001751563.2:n.216+33658G>A | ||
| XR_001751565.2:n.2400G>A | ||
| XR_429537.4:n.216+33658G>A |