Linked Data
ClinVar Variation Id:
1657433
dbSNP Id:
rs777458923
ExAC:
17:4805619 A / G
gnomAD v2:
17-4805619-A-G
gnomAD v4:
17-4902324-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.4902324A>G , CM000679.2:g.4902324A>G | GRCh38 |
| NC_000017.10:g.4805619A>G , CM000679.1:g.4805619A>G | GRCh37 |
| NC_000017.9:g.4746398A>G | NCBI36 |
| NG_008029.2:g.5752T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381365.4:c.*1791A>G (C17orf107) MANE Select | ENSP00000370770.3:n.*1791A>G | |
| ENST00000649488.2:c.237T>C (CHRNE) MANE Select | ENSP00000497829.1:p.Asp79= | |
| ENST00000649830.1:c.-697T>C (CHRNE) | ENSP00000496907.1:n.-697T>C | |
| ENST00000293780.4:c.237T>C (CHRNE) | ENSP00000293780.4:p.Asp79= | |
| ENST00000381365.3:c.*1791A>G (C17orf107) | ENSP00000370770.3:n.*1791A>G | |
| ENST00000575637.1:n.58T>C (CHRNE) | ||
| NM_000080.3:c.237T>C (CHRNE) | NP_000071.1:p.Asp79= | |
| NM_001145536.1:c.*1791A>G (C17orf107) | NP_001139008.1:n.*1791A>G | |
| XM_011523612.1:c.546+1818A>G (C17orf107) | XP_011521914.1:n.546+1818A>G | |
| XM_011523631.1:c.237T>C (CHRNE) | XP_011521933.1:p.Asp79= | |
| NM_000080.4:c.237T>C (CHRNE) MANE Select | NP_000071.1:p.Asp79= | |
| XM_017024115.1:c.201T>C (CHRNE) | XP_016879604.1:p.Asp67= | |
| XR_001752421.1:n.1082T>C (CHRNE) | ||
| NM_001145536.2:c.*1791A>G (C17orf107) MANE Select | NP_001139008.1:n.*1791A>G |