MyVariant.info:
GRCh37
chr2:g.39278378T>A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.39051237T>A , CM000664.2:g.39051237T>A | GRCh38 |
| NC_000002.11:g.39278378T>A , CM000664.1:g.39278378T>A | GRCh37 |
| NC_000002.10:g.39131882T>A | NCBI36 |
| NG_007530.1:g.74227A>T , LRG_754:g.74227A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000461545.2:n.798A>T | ||
| ENST00000472480.2:n.651A>T | ||
| ENST00000685782.1:n.1609A>T | ||
| ENST00000689668.1:n.778A>T | ||
| ENST00000690679.1:c.871A>T | ||
| ENST00000690876.1:c.771A>T | ENSP00000508955.1:p.Val257= | |
| ENST00000691229.1:c.771A>T | ENSP00000510437.1:p.Val257= | |
| ENST00000692089.1:c.771A>T | ENSP00000508626.1:p.Val257= | |
| ENST00000402219.8:c.771A>T MANE Select | ENSP00000384675.2:p.Val257= | |
| ENST00000395038.6:c.771A>T | ENSP00000378479.2:p.Val257= | |
| ENST00000402219.6:c.771A>T | ENSP00000384675.2:p.Val257= | |
| ENST00000426016.5:c.771A>T | ENSP00000387784.1:p.Val257= | |
| ENST00000461545.1:n.121A>T | ||
| NM_005633.3:c.771A>T , LRG_754t1:c.771A>T | NP_005624.2:p.Val257= | |
| XM_005264515.3:c.771A>T | XP_005264572.1:p.Val257= | |
| XM_011533060.1:c.864A>T | XP_011531362.1:p.Val288= | |
| XM_011533061.1:c.864A>T | XP_011531363.1:p.Val288= | |
| XM_011533062.1:c.750A>T | XP_011531364.1:p.Val250= | |
| XM_011533063.1:c.747A>T | XP_011531365.1:p.Val249= | |
| XM_011533064.1:c.600A>T | XP_011531366.1:p.Val200= | |
| XM_011533065.1:c.864A>T | XP_011531367.1:p.Val288= | |
| XM_005264515.4:c.771A>T | XP_005264572.1:p.Val257= | |
| XM_011533062.2:c.750A>T | XP_011531364.1:p.Val250= | |
| XM_011533064.2:c.600A>T | XP_011531366.1:p.Val200= | |
| NM_001382394.1:c.750A>T | NP_001369323.1:p.Val250= | |
| NM_001382395.1:c.771A>T | NP_001369324.1:p.Val257= | |
| NM_005633.4:c.771A>T MANE Select | NP_005624.2:p.Val257= |