Linked Data
dbSNP Id:
rs4810485
gnomAD v2:
20-44747947-T-G
gnomAD v3:
20-46119308-T-G
gnomAD v4:
20-46119308-T-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.46119308T>G , CM000682.2:g.46119308T>G | GRCh38 |
| NC_000020.10:g.44747947T>G , CM000682.1:g.44747947T>G | GRCh37 |
| NC_000020.9:g.44181354T>G | NCBI36 |
| NG_007279.1:g.6042T>G , LRG_40:g.6042T>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000477696.6:c.51+914T>G | ENSP00000512095.1:n.51+914T>G | |
| ENST00000489304.6:c.51+914T>G | ENSP00000512096.1:n.51+914T>G | |
| ENST00000695669.1:n.124+914T>G | ||
| ENST00000695670.1:n.110+914T>G | ||
| ENST00000695671.1:c.51+914T>G | ENSP00000512093.1:n.51+914T>G | |
| ENST00000695672.1:n.55+914T>G | ||
| ENST00000372285.8:c.51+914T>G MANE Select | ENSP00000361359.3:n.51+914T>G | |
| ENST00000372276.7:c.51+914T>G | ENSP00000361350.3:n.51+914T>G | |
| ENST00000372285.7:c.51+914T>G | ENSP00000361359.3:n.51+914T>G | |
| ENST00000466205.5:c.47+914T>G | ||
| ENST00000477696.5:n.22+914T>G | ||
| ENST00000489304.5:n.44+914T>G | ||
| ENST00000620709.4:c.51+914T>G | ENSP00000484074.1:n.51+914T>G | |
| NM_001250.5:c.51+914T>G | NP_001241.1:n.51+914T>G | |
| NM_001302753.1:c.51+914T>G | NP_001289682.1:n.51+914T>G | |
| NM_152854.3:c.51+914T>G | NP_690593.1:n.51+914T>G | |
| NR_126502.1:n.141+914T>G | ||
| XM_005260617.2:c.51+914T>G | XP_005260674.1:n.51+914T>G | |
| XM_005260619.2:c.51+914T>G | XP_005260676.1:n.51+914T>G | |
| XM_011529109.1:c.51+914T>G | XP_011527411.1:n.51+914T>G | |
| XR_936660.1:n.145+914T>G | ||
| NM_001322421.1:c.51+914T>G | NP_001309350.1:n.51+914T>G | |
| NM_001322422.1:c.51+914T>G | NP_001309351.1:n.51+914T>G | |
| NM_001362758.1:c.51+914T>G | NP_001349687.1:n.51+914T>G | |
| NR_136327.1:n.141+914T>G | ||
| XM_005260619.3:c.51+914T>G | XP_005260676.1:n.51+914T>G | |
| XM_011529109.2:c.51+914T>G | XP_011527411.1:n.51+914T>G | |
| XM_017028135.1:c.51+914T>G | XP_016883624.1:n.51+914T>G | |
| XM_017028136.1:c.51+914T>G | XP_016883625.1:n.51+914T>G | |
| NM_001250.6:c.51+914T>G MANE Select | NP_001241.1:n.51+914T>G | |
| NM_001302753.2:c.51+914T>G | NP_001289682.1:n.51+914T>G | |
| NM_001322421.2:c.51+914T>G | NP_001309350.1:n.51+914T>G | |
| NM_001322422.2:c.51+914T>G | NP_001309351.1:n.51+914T>G | |
| NM_001362758.2:c.51+914T>G | NP_001349687.1:n.51+914T>G | |
| NM_152854.4:c.51+914T>G | NP_690593.1:n.51+914T>G | |
| NR_126502.2:n.81+914T>G | ||
| NR_136327.2:n.81+914T>G |