Linked Data
dbSNP Id:
rs10106137
gnomAD v2:
8-75527633-C-A
gnomAD v3:
8-74615398-C-A
gnomAD v4:
8-74615398-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.74615398C>A , CM000670.2:g.74615398C>A | GRCh38 |
| NC_000008.10:g.75527633C>A , CM000670.1:g.75527633C>A | GRCh37 |
| NC_000008.9:g.75690188C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| NR_033830.1:n.131+2458C>A (MIR2052HG) | ||
| XR_929054.1:n.345+1362G>T (LINC03071) | ||
| XR_929055.1:n.165-2832G>T (LINC03071) | ||
| XR_929056.1:n.345+1362G>T (LINC03071) | ||
| XR_929057.1:n.222+1362G>T (LINC03071) | ||
| XR_001745957.1:n.628+1362G>T (LINC03071) | ||
| XR_001745958.1:n.448-2832G>T (LINC03071) | ||
| XR_001745960.1:n.222+1362G>T (LINC03071) | ||
| XR_002956714.1:n.628+1362G>T (LINC03071) |