Linked Data
dbSNP Id:
rs1318016584
gnomAD v2:
2-25457098-T-A
gnomAD v3:
2-25234229-T-A
gnomAD v4:
2-25234229-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.25234229T>A , CM000664.2:g.25234229T>A | GRCh38 |
| NC_000002.11:g.25457098T>A , CM000664.1:g.25457098T>A | GRCh37 |
| NC_000002.10:g.25310602T>A | NCBI36 |
| NG_029465.2:g.113362A>T , LRG_459:g.113362A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683393.1:c.1935A>T | ENSP00000508654.1:n.1935A>T | |
| ENST00000683760.1:c.*50A>T | ENSP00000507765.1:n.*50A>T | |
| ENST00000321117.10:c.*50A>T MANE Select | ENSP00000324375.5:n.*50A>T | |
| ENST00000264709.7:c.*50A>T | ENSP00000264709.3:n.*50A>T | |
| ENST00000321117.9:c.*50A>T | ENSP00000324375.5:n.*50A>T | |
| ENST00000380746.8:c.*50A>T | ENSP00000370122.4:n.*50A>T | |
| ENST00000380756.7:c.*642A>T | ENSP00000370132.3:n.*642A>T | |
| ENST00000402667.1:c.*50A>T | ENSP00000384237.1:n.*50A>T | |
| NM_022552.4:c.*50A>T , LRG_459t1:c.*50A>T | NP_072046.2:n.*50A>T | |
| NM_153759.3:c.*50A>T , LRG_459t2:c.*50A>T | NP_715640.2:n.*50A>T | |
| NM_175629.2:c.*50A>T , LRG_459t4:c.*50A>T | NP_783328.1:n.*50A>T | |
| XM_005264175.3:c.*50A>T | XP_005264232.1:n.*50A>T | |
| XM_005264177.3:c.*50A>T | XP_005264234.1:n.*50A>T | |
| XM_006711958.2:c.*50A>T | XP_006712021.1:n.*50A>T | |
| XM_011532662.1:c.*50A>T | XP_011530964.1:n.*50A>T | |
| XM_011532663.1:c.*50A>T | XP_011530965.1:n.*50A>T | |
| XM_011532665.1:c.*50A>T | XP_011530967.1:n.*50A>T | |
| XM_011532666.1:c.*50A>T | XP_011530968.1:n.*50A>T | |
| XM_011532667.1:c.*50A>T | XP_011530969.1:n.*50A>T | |
| NM_001320893.1:c.*50A>T | NP_001307822.1:n.*50A>T | |
| NR_135490.1:n.3326A>T | ||
| XM_005264175.5:c.*50A>T | XP_005264232.1:n.*50A>T | |
| XM_005264177.4:c.*50A>T | XP_005264234.1:n.*50A>T | |
| XM_011532662.2:c.*50A>T | XP_011530964.1:n.*50A>T | |
| XM_011532663.2:c.*50A>T | XP_011530965.1:n.*50A>T | |
| XM_011532666.2:c.*50A>T | XP_011530968.1:n.*50A>T | |
| XM_011532667.3:c.*50A>T | XP_011530969.1:n.*50A>T | |
| XM_017003526.1:c.*50A>T | XP_016859015.1:n.*50A>T | |
| XM_017003527.1:c.*50A>T | XP_016859016.1:n.*50A>T | |
| XR_001738657.1:n.2996A>T | ||
| NM_001375819.1:c.*50A>T | NP_001362748.1:n.*50A>T | |
| NR_135490.2:n.3219A>T | ||
| NM_022552.5:c.*50A>T MANE Select | NP_072046.2:n.*50A>T |