Linked Data
dbSNP Id:
rs1362525333
gnomAD v2:
2-39250337-T-A
gnomAD v3:
2-39023196-T-A
gnomAD v4:
2-39023196-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.39023196T>A , CM000664.2:g.39023196T>A | GRCh38 |
| NC_000002.11:g.39250337T>A , CM000664.1:g.39250337T>A | GRCh37 |
| NC_000002.10:g.39103841T>A | NCBI36 |
| NG_007530.1:g.102268A>T , LRG_754:g.102268A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000472480.2:n.1112A>T | ||
| ENST00000685279.1:c.-2A>T | ENSP00000509424.1:n.-2A>T | |
| ENST00000688043.1:n.1453A>T | ||
| ENST00000689668.1:n.1239A>T | ||
| ENST00000690679.1:c.1419A>T | ||
| ENST00000690876.1:c.1121A>T | ENSP00000508955.1:p.Gln374Leu | |
| ENST00000691229.1:c.1121A>T | ENSP00000510437.1:p.Gln374Leu | |
| ENST00000692089.1:c.1121A>T | ENSP00000508626.1:p.Gln374Leu | |
| ENST00000692620.1:c.-2A>T | ENSP00000509311.1:n.-2A>T | |
| ENST00000402219.8:c.1232A>T MANE Select | ENSP00000384675.2:p.Gln411Leu | |
| ENST00000395038.6:c.1232A>T | ENSP00000378479.2:p.Gln411Leu | |
| ENST00000402219.6:c.1232A>T | ENSP00000384675.2:p.Gln411Leu | |
| ENST00000426016.5:c.1232A>T | ENSP00000387784.1:p.Gln411Leu | |
| ENST00000472480.1:n.76A>T | ||
| NM_005633.3:c.1232A>T , LRG_754t1:c.1232A>T | NP_005624.2:p.Gln411Leu | |
| XM_005264515.3:c.1232A>T | XP_005264572.1:p.Gln411Leu | |
| XM_011533060.1:c.1325A>T | XP_011531362.1:p.Gln442Leu | |
| XM_011533061.1:c.1325A>T | XP_011531363.1:p.Gln442Leu | |
| XM_011533062.1:c.1211A>T | XP_011531364.1:p.Gln404Leu | |
| XM_011533063.1:c.1208A>T | XP_011531365.1:p.Gln403Leu | |
| XM_011533064.1:c.1061A>T | XP_011531366.1:p.Gln354Leu | |
| XM_011533065.1:c.1325A>T | XP_011531367.1:p.Gln442Leu | |
| XM_011533066.1:c.167A>T | XP_011531368.1:p.Gln56Leu | |
| XM_005264515.4:c.1232A>T | XP_005264572.1:p.Gln411Leu | |
| XM_011533062.2:c.1211A>T | XP_011531364.1:p.Gln404Leu | |
| XM_011533064.2:c.1061A>T | XP_011531366.1:p.Gln354Leu | |
| NM_001382394.1:c.1211A>T | NP_001369323.1:p.Gln404Leu | |
| NM_001382395.1:c.1232A>T | NP_001369324.1:p.Gln411Leu | |
| NM_005633.4:c.1232A>T MANE Select | NP_005624.2:p.Gln411Leu |