Linked Data
ClinVar Variation Id:
324162
dbSNP Id:
rs201961765
ExAC:
17:56290388 G / A
gnomAD v2:
17-56290388-G-A
gnomAD v3:
17-58213027-G-A
gnomAD v4:
17-58213027-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.58213027G>A , CM000679.2:g.58213027G>A | GRCh38 |
| NC_000017.10:g.56290388G>A , CM000679.1:g.56290388G>A | GRCh37 |
| NC_000017.9:g.53645387G>A | NCBI36 |
| NG_013032.1:g.11579C>T , LRG_687:g.11579C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000313863.11:c.813C>T | ENSP00000316631.6:p.His271= | |
| ENST00000393119.7:c.813C>T MANE Select | ENSP00000376827.2:p.His271= | |
| ENST00000537529.7:c.384C>T | ENSP00000442096.3:p.His128= | |
| ENST00000580127.6:c.813C>T | ENSP00000462423.2:p.His271= | |
| ENST00000581761.6:c.813C>T | ENSP00000462129.2:p.His271= | |
| ENST00000585134.2:c.813C>T | ENSP00000463826.2:p.His271= | |
| ENST00000675753.2:c.*432C>T | ENSP00000502156.1:n.*432C>T | |
| ENST00000676787.1:c.684C>T | ENSP00000503999.1:p.His228= | |
| ENST00000676975.1:c.678C>T | ENSP00000503970.1:n.678C>T | |
| ENST00000677076.1:n.2087C>T | ||
| ENST00000677111.1:c.813C>T | ENSP00000504282.1:p.His271= | |
| ENST00000677160.1:n.2087C>T | ||
| ENST00000677416.1:n.838C>T | ||
| ENST00000677475.1:n.2764C>T | ||
| ENST00000677486.1:c.*157C>T | ENSP00000503852.1:n.*157C>T | |
| ENST00000677546.1:c.*157C>T | ENSP00000504043.1:n.*157C>T | |
| ENST00000677709.1:n.838C>T | ||
| ENST00000678011.1:n.838C>T | ||
| ENST00000678211.1:n.2862C>T | ||
| ENST00000678432.1:c.*432C>T | ENSP00000504452.1:n.*432C>T | |
| ENST00000678463.1:c.813C>T | ENSP00000502984.1:p.His271= | |
| ENST00000678481.1:n.614C>T | ||
| ENST00000678568.1:c.*220C>T | ENSP00000504754.1:n.*220C>T | |
| ENST00000678641.1:c.*157C>T | ENSP00000503159.1:n.*157C>T | |
| ENST00000678928.1:n.2440C>T | ||
| ENST00000679081.1:n.2829C>T | ||
| ENST00000313863.10:c.813C>T | ENSP00000316631.6:p.His271= | |
| ENST00000393119.6:c.813C>T | ENSP00000376827.2:p.His271= | |
| ENST00000393120.6:c.*220C>T | ENSP00000376828.2:n.*220C>T | |
| ENST00000537529.6:c.783C>T | ENSP00000442096.2:p.His261= | |
| ENST00000577824.5:c.290C>T | ||
| ENST00000581761.5:c.*220C>T | ENSP00000462129.1:n.*220C>T | |
| ENST00000585134.1:c.36C>T | ENSP00000463826.1:p.His12= | |
| NM_001165927.1:c.783C>T , LRG_687t2:c.783C>T | NP_001159399.1:p.His261= | |
| NM_017777.3:c.813C>T , LRG_687t1:c.813C>T | NP_060247.2:p.His271= | |
| XM_005257483.3:c.813C>T | XP_005257540.1:p.His271= | |
| XM_005257485.3:c.384C>T | XP_005257542.1:p.His128= | |
| XM_005257486.3:c.204C>T | XP_005257543.1:p.His68= | |
| XM_006721965.2:c.204C>T | XP_006722028.1:p.His68= | |
| XM_011524957.1:c.822C>T | XP_011523259.1:p.His274= | |
| XM_011524958.1:c.822C>T | XP_011523260.1:p.His274= | |
| XM_011524959.1:c.822C>T | XP_011523261.1:p.His274= | |
| XM_011524960.1:c.822C>T | XP_011523262.1:p.His274= | |
| XR_934494.1:n.870C>T | ||
| NM_001321268.1:c.204C>T | NP_001308197.1:p.His68= | |
| NM_001321269.1:c.813C>T | NP_001308198.1:p.His271= | |
| NM_001330397.1:c.813C>T | NP_001317326.1:p.His271= | |
| XM_005257485.4:c.384C>T | XP_005257542.1:p.His128= | |
| XM_006721965.3:c.204C>T | XP_006722028.1:p.His68= | |
| XM_011524957.2:c.822C>T | XP_011523259.1:p.His274= | |
| XM_011524958.2:c.822C>T | XP_011523260.1:p.His274= | |
| XM_011524959.2:c.822C>T | XP_011523261.1:p.His274= | |
| XM_011524960.2:c.822C>T | XP_011523262.1:p.His274= | |
| XM_017024804.2:c.813C>T | XP_016880293.1:p.His271= | |
| XM_017024805.1:c.384C>T | XP_016880294.1:p.His128= | |
| XR_002958042.1:n.867C>T | ||
| NM_001321268.2:c.204C>T | NP_001308197.1:p.His68= | |
| NM_001321269.2:c.813C>T | NP_001308198.1:p.His271= | |
| NM_001330397.2:c.813C>T | NP_001317326.1:p.His271= | |
| NM_017777.4:c.813C>T MANE Select | NP_060247.2:p.His271= |