Linked Data
ClinVar Variation Id:
582514
dbSNP Id:
rs781427897
ExAC:
16:68835772 C / A
gnomAD v2:
16-68835772-C-A
gnomAD v4:
16-68801869-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68801869C>A , CM000678.2:g.68801869C>A | GRCh38 |
| NC_000016.9:g.68835772C>A , CM000678.1:g.68835772C>A | GRCh37 |
| NC_000016.8:g.67393273C>A | NCBI36 |
| NG_008021.1:g.69578C>A , LRG_301:g.69578C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261769.10:c.363C>A MANE Select | ENSP00000261769.4:p.His121Gln | |
| ENST00000261769.9:c.363C>A | ENSP00000261769.4:p.His121Gln | |
| ENST00000422392.6:c.363C>A | ENSP00000414946.2:p.His121Gln | |
| ENST00000561751.1:c.130C>A | ||
| ENST00000562836.5:n.434C>A | ||
| ENST00000564676.5:n.645C>A | ||
| ENST00000564745.1:n.358C>A | ||
| ENST00000566510.5:c.363C>A | ENSP00000458139.1:p.His121Gln | |
| ENST00000566612.5:c.363C>A | ENSP00000454782.1:p.His121Gln | |
| ENST00000611625.4:c.363C>A | ENSP00000481063.1:p.His121Gln | |
| ENST00000612417.4:c.363C>A | ENSP00000478360.1:p.His121Gln | |
| ENST00000621016.4:c.363C>A | ENSP00000480664.1:p.His121Gln | |
| NM_004360.3:c.363C>A , LRG_301t1:c.363C>A | NP_004351.1:p.His121Gln | |
| XM_011523488.1:c.-373C>A | XP_011521790.1:n.-373C>A | |
| XM_011523489.1:c.-373C>A | XP_011521791.1:n.-373C>A | |
| NM_001317184.1:c.363C>A | NP_001304113.1:p.His121Gln | |
| NM_001317185.1:c.-1253C>A | NP_001304114.1:n.-1253C>A | |
| NM_001317186.1:c.-1457C>A | NP_001304115.1:n.-1457C>A | |
| NM_004360.4:c.363C>A | NP_004351.1:p.His121Gln | |
| NM_004360.5:c.363C>A MANE Select | NP_004351.1:p.His121Gln | |
| NM_001317184.2:c.363C>A | NP_001304113.1:p.His121Gln | |
| NM_001317185.2:c.-1253C>A | NP_001304114.1:n.-1253C>A | |
| NM_001317186.2:c.-1457C>A | NP_001304115.1:n.-1457C>A |