Linked Data
dbSNP Id:
rs4887067
gnomAD v2:
15-78886947-G-A
gnomAD v3:
15-78594605-G-A
gnomAD v4:
15-78594605-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.78594605G>A , CM000677.2:g.78594605G>A | GRCh38 |
| NC_000015.9:g.78886947G>A , CM000677.1:g.78886947G>A | GRCh37 |
| NC_000015.8:g.76674002G>A | NCBI36 |
| NG_016143.1:g.31691C>T | |
| NG_023328.1:g.34086G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000299565.9:c.*1352G>A (CHRNA5) MANE Select | ENSP00000299565.5:n.*1352G>A | |
| ENST00000348639.7:c.1390-1414C>T (CHRNA3) | ENSP00000267951.4:n.1390-1414C>T | |
| ENST00000559002.5:n.194-1414C>T (CHRNA3) | ||
| ENST00000559658.5:c.*65-594C>T (CHRNA3) | ENSP00000452896.1:n.*65-594C>T | |
| NM_000745.3:c.*1352G>A (CHRNA5) | NP_000736.2:n.*1352G>A | |
| NM_001166694.1:c.1390-1414C>T (CHRNA3) | NP_001160166.1:n.1390-1414C>T | |
| NM_001307945.1:c.*1489G>A (CHRNA5) | NP_001294874.1:n.*1489G>A | |
| NR_046313.1:n.2084-594C>T (CHRNA3) | ||
| NM_001166694.2:c.1390-1414C>T (CHRNA3) | NP_001160166.1:n.1390-1414C>T | |
| NM_001307945.2:c.*1489G>A (CHRNA5) | NP_001294874.1:n.*1489G>A | |
| NR_046313.2:n.1785-594C>T (CHRNA3) | ||
| NM_000745.4:c.*1352G>A (CHRNA5) MANE Select | NP_000736.2:n.*1352G>A | |
| NM_001395171.1:c.*1489G>A (CHRNA5) | NP_001382100.1:n.*1489G>A | |
| NM_001395172.1:c.*1352G>A (CHRNA5) | NP_001382101.1:n.*1352G>A | |
| NM_001395173.1:c.*1489G>A (CHRNA5) | NP_001382102.1:n.*1489G>A | |
| NM_001395174.1:c.*1489G>A (CHRNA5) | NP_001382103.1:n.*1489G>A | |
| NM_001395175.1:c.*1489G>A (CHRNA5) | NP_001382104.1:n.*1489G>A |