MyVariant.info:
GRCh37
chr2:g.39241932T>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.39014791T>C , CM000664.2:g.39014791T>C | GRCh38 |
| NC_000002.11:g.39241932T>C , CM000664.1:g.39241932T>C | GRCh37 |
| NC_000002.10:g.39095436T>C | NCBI36 |
| NG_007530.1:g.110673A>G , LRG_754:g.110673A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000685279.1:c.681A>G | ENSP00000509424.1:p.Gln227= | |
| ENST00000688043.1:n.2135A>G | ||
| ENST00000689668.1:n.1921A>G | ||
| ENST00000690876.1:c.1803A>G | ENSP00000508955.1:p.Gln601= | |
| ENST00000691229.1:c.1803A>G | ENSP00000510437.1:p.Gln601= | |
| ENST00000692089.1:c.1803A>G | ENSP00000508626.1:p.Gln601= | |
| ENST00000692620.1:c.681A>G | ENSP00000509311.1:p.Gln227= | |
| ENST00000402219.8:c.1914A>G MANE Select | ENSP00000384675.2:p.Gln638= | |
| ENST00000395038.6:c.1914A>G | ENSP00000378479.2:p.Gln638= | |
| ENST00000402219.6:c.1914A>G | ENSP00000384675.2:p.Gln638= | |
| ENST00000426016.5:c.1914A>G | ENSP00000387784.1:p.Gln638= | |
| NM_005633.3:c.1914A>G , LRG_754t1:c.1914A>G | NP_005624.2:p.Gln638= | |
| XM_005264515.3:c.1914A>G | XP_005264572.1:p.Gln638= | |
| XM_011533060.1:c.2007A>G | XP_011531362.1:p.Gln669= | |
| XM_011533061.1:c.2007A>G | XP_011531363.1:p.Gln669= | |
| XM_011533062.1:c.1893A>G | XP_011531364.1:p.Gln631= | |
| XM_011533063.1:c.1890A>G | XP_011531365.1:p.Gln630= | |
| XM_011533064.1:c.1743A>G | XP_011531366.1:p.Gln581= | |
| XM_011533065.1:c.2007A>G | XP_011531367.1:p.Gln669= | |
| XM_011533066.1:c.849A>G | XP_011531368.1:p.Gln283= | |
| XM_005264515.4:c.1914A>G | XP_005264572.1:p.Gln638= | |
| XM_011533062.2:c.1893A>G | XP_011531364.1:p.Gln631= | |
| XM_011533064.2:c.1743A>G | XP_011531366.1:p.Gln581= | |
| NM_001382394.1:c.1893A>G | NP_001369323.1:p.Gln631= | |
| NM_001382395.1:c.1914A>G | NP_001369324.1:p.Gln638= | |
| NM_005633.4:c.1914A>G MANE Select | NP_005624.2:p.Gln638= |