ClinVar Allele:
ClinVar Variation:
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.144401292G>A , CM000664.2:g.144401292G>A | GRCh38 |
| NC_000002.11:g.145158859G>A , CM000664.1:g.145158859G>A | GRCh37 |
| NC_000002.10:g.144875329G>A | NCBI36 |
| NG_016431.1:g.124100C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000689298.1:c.*672C>T | ENSP00000508434.1:n.*672C>T | |
| ENST00000440875.6:c.46C>T | ENSP00000475553.3:p.Gln16Ter | |
| ENST00000627532.3:c.823C>T MANE Select | ENSP00000487174.1:p.Gln275Ter | |
| ENST00000636026.2:c.823C>T | ENSP00000490776.1:p.Gln275Ter | |
| ENST00000636179.1:n.792C>T | ||
| ENST00000636413.1:c.487C>T | ENSP00000490508.1:p.Gln163Ter | |
| ENST00000636471.1:c.823C>T | ENSP00000490317.1:p.Gln275Ter | |
| ENST00000636732.2:c.*540C>T | ENSP00000490175.1:n.*540C>T | |
| ENST00000636820.1:n.923C>T | ||
| ENST00000637045.1:c.487C>T | ENSP00000490141.1:p.Gln163Ter | |
| ENST00000637267.2:c.823C>T | ENSP00000490293.2:p.Gln275Ter | |
| ENST00000637304.1:c.487C>T | ENSP00000490872.1:p.Gln163Ter | |
| ENST00000638007.1:c.487C>T | ENSP00000490723.1:p.Gln163Ter | |
| ENST00000638087.1:c.487C>T | ENSP00000490673.1:p.Gln163Ter | |
| ENST00000638128.1:c.46C>T | ENSP00000490934.1:p.Gln16Ter | |
| ENST00000675069.1:c.-133-2442C>T | ENSP00000502467.1:n.-133-2442C>T | |
| ENST00000675145.1:n.1371C>T | ||
| ENST00000303660.8:c.820C>T | ENSP00000302501.4:p.Gln274Ter | |
| ENST00000392861.6:c.907C>T | ENSP00000376601.3:p.Gln303Ter | |
| ENST00000409487.7:c.823C>T | ENSP00000386854.2:p.Gln275Ter | |
| ENST00000419938.5:c.562C>T | ENSP00000394777.2:p.Gln188Ter | |
| ENST00000427902.5:c.910C>T | ENSP00000395496.2:p.Gln304Ter | |
| ENST00000440875.5:c.808C>T | ENSP00000475553.2:p.Gln270Ter | |
| ENST00000539609.7:c.751C>T | ENSP00000443792.2:p.Gln251Ter | |
| ENST00000558170.6:c.823C>T | ENSP00000454157.1:p.Gln275Ter | |
| ENST00000627532.2:c.823C>T | ENSP00000487174.1:p.Gln275Ter | |
| NM_001171653.1:c.751C>T | NP_001165124.1:p.Gln251Ter | |
| NM_014795.3:c.823C>T | NP_055610.1:p.Gln275Ter | |
| XM_006712881.2:c.823C>T | XP_006712944.1:p.Gln275Ter | |
| XM_006712882.2:c.823C>T | XP_006712945.1:p.Gln275Ter | |
| XM_011512231.1:c.814C>T | XP_011510533.1:p.Gln272Ter | |
| XM_011512232.1:c.802C>T | XP_011510534.1:p.Gln268Ter | |
| NM_014795.4:c.823C>T MANE Select | NP_055610.1:p.Gln275Ter | |
| NM_001171653.2:c.751C>T | NP_001165124.1:p.Gln251Ter |