Linked Data
dbSNP Id:
rs206936
gnomAD v2:
6-34302869-A-G
gnomAD v3:
6-34335092-A-G
gnomAD v4:
6-34335092-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.34335092A>G , CM000668.2:g.34335092A>G | GRCh38 |
| NC_000006.11:g.34302869A>G , CM000668.1:g.34302869A>G | GRCh37 |
| NC_000006.10:g.34410847A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000605528.2:c.384-39407T>C (RPS10-NUDT3) | ||
| ENST00000607016.2:c.210+6770T>C (NUDT3) MANE Select | ENSP00000476119.1:n.210+6770T>C | |
| ENST00000639725.1:c.567+6770T>C (RPS10-NUDT3) | ENSP00000492441.1:n.567+6770T>C | |
| ENST00000639877.1:c.567+6770T>C (RPS10-NUDT3) | ENSP00000491891.1:n.567+6770T>C | |
| ENST00000605528.1:c.567+6770T>C (RPS10-NUDT3) | ENSP00000475027.1:n.567+6770T>C | |
| ENST00000607016.1:c.210+6770T>C (NUDT3) | ENSP00000476119.1:n.210+6770T>C | |
| NM_001202470.2:c.567+6770T>C (RPS10-NUDT3) | NP_001189399.1:n.567+6770T>C | |
| NM_006703.3:c.210+6770T>C (NUDT3) | NP_006694.1:n.210+6770T>C | |
| NM_006703.4:c.210+6770T>C (NUDT3) MANE Select | NP_006694.1:n.210+6770T>C | |
| NM_001202470.3:c.567+6770T>C (RPS10-NUDT3) | NP_001189399.1:n.567+6770T>C |