Linked Data
dbSNP Id:
rs994528922
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.74600826A>G , CM000670.2:g.74600826A>G | GRCh38 |
| NC_000008.10:g.75513061A>G , CM000670.1:g.75513061A>G | GRCh37 |
| NC_000008.9:g.75675616A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| NR_033830.1:n.43+918A>G (MIR2052HG) | ||
| XR_929054.1:n.459-10449T>C (LINC03071) | ||
| XR_929055.1:n.278-10449T>C (LINC03071) | ||
| XR_929057.1:n.336-10449T>C (LINC03071) | ||
| XR_001745957.1:n.742-10449T>C (LINC03071) | ||
| XR_001745958.1:n.561-10449T>C (LINC03071) | ||
| XR_001745960.1:n.336-10449T>C (LINC03071) |