Linked Data
ClinVar Variation Id:
510879
dbSNP Id:
rs141065708
ExAC:
16:89590553 C / T
gnomAD v2:
16-89590553-C-T
gnomAD v3:
16-89524145-C-T
gnomAD v4:
16-89524145-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89524145C>T , CM000678.2:g.89524145C>T | GRCh38 |
| NC_000016.9:g.89590553C>T , CM000678.1:g.89590553C>T | GRCh37 |
| NC_000016.8:g.88118054C>T | NCBI36 |
| NG_008082.1:g.20749C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268704.7:c.516C>T | ENSP00000268704.3:p.His172= | |
| ENST00000562775.2:n.380C>T | ||
| ENST00000564047.2:n.525C>T | ||
| ENST00000564409.2:c.285C>T | ENSP00000495297.1:p.His95= | |
| ENST00000566371.6:c.516C>T | ENSP00000454475.2:p.His172= | |
| ENST00000642334.1:c.389C>T | ||
| ENST00000642371.1:c.448C>T | ||
| ENST00000642436.1:n.388+11108C>T | ||
| ENST00000643105.1:c.436C>T | ||
| ENST00000643178.1:n.164C>T | ||
| ENST00000643307.1:c.516C>T | ENSP00000495673.1:p.His172= | |
| ENST00000643345.1:c.377-4990C>T | ENSP00000493982.1:n.377-4990C>T | |
| ENST00000643496.1:n.333C>T | ||
| ENST00000643649.1:c.516C>T | ENSP00000494806.1:p.His172= | |
| ENST00000643668.1:c.*544C>T | ENSP00000494903.1:n.*544C>T | |
| ENST00000643724.1:c.516C>T | ENSP00000496335.1:p.His172= | |
| ENST00000643954.1:c.254C>T | ||
| ENST00000643957.1:c.677C>T | ENSP00000494246.1:n.677C>T | |
| ENST00000644210.1:c.516C>T | ENSP00000495675.1:p.His172= | |
| ENST00000644225.1:n.533C>T | ||
| ENST00000644498.1:c.516C>T | ENSP00000496244.1:p.His172= | |
| ENST00000644671.1:c.179C>T | ||
| ENST00000644748.1:n.1947C>T | ||
| ENST00000644781.1:c.516C>T | ENSP00000495473.1:p.His172= | |
| ENST00000644901.1:c.516C>T | ENSP00000493797.1:p.His172= | |
| ENST00000645042.1:c.516C>T | ENSP00000493908.1:p.His172= | |
| ENST00000645063.1:c.516C>T | ENSP00000493590.1:p.His172= | |
| ENST00000645354.1:c.431C>T | ||
| ENST00000645533.1:c.516C>T | ENSP00000495690.1:p.His172= | |
| ENST00000645818.2:c.516C>T MANE Select | ENSP00000495795.2:p.His172= | |
| ENST00000645897.1:c.516C>T | ENSP00000495293.1:p.His172= | |
| ENST00000645977.1:n.531C>T | ||
| ENST00000646263.1:c.516C>T | ENSP00000494119.1:p.His172= | |
| ENST00000646303.1:c.384C>T | ENSP00000494160.1:p.His128= | |
| ENST00000646399.1:c.199C>T | ||
| ENST00000646445.1:c.182+11108C>T | ||
| ENST00000646531.1:c.516C>T | ENSP00000495185.1:p.His172= | |
| ENST00000646589.1:c.377-6538C>T | ENSP00000494739.1:n.377-6538C>T | |
| ENST00000646716.1:c.376+11108C>T | ENSP00000495593.1:n.376+11108C>T | |
| ENST00000646826.1:c.516C>T | ENSP00000495123.1:p.His172= | |
| ENST00000646930.1:c.516C>T | ENSP00000495219.1:p.His172= | |
| ENST00000646958.1:n.466C>T | ||
| ENST00000647032.1:c.131C>T | ||
| ENST00000647079.1:c.108C>T | ENSP00000495967.1:p.His36= | |
| ENST00000647227.1:c.279C>T | ||
| ENST00000268704.6:c.516C>T | ENSP00000268704.2:p.His172= | |
| ENST00000341316.6:c.516C>T | ENSP00000341157.2:p.His172= | |
| ENST00000562775.1:n.1426C>T | ||
| ENST00000566371.5:c.384C>T | ENSP00000454475.1:p.His128= | |
| ENST00000620811.4:c.-1061C>T | ENSP00000478030.1:n.-1061C>T | |
| NM_003119.3:c.516C>T | NP_003110.1:p.His172= | |
| NM_199367.2:c.516C>T | NP_955399.1:p.His172= | |
| XM_005256321.3:c.516C>T | XP_005256378.1:p.His172= | |
| XM_006721264.2:c.516C>T | XP_006721327.1:p.His172= | |
| XM_011523306.1:c.516C>T | XP_011521608.1:p.His172= | |
| XM_011523307.1:c.516C>T | XP_011521609.1:p.His172= | |
| NM_001363850.1:c.516C>T | NP_001350779.1:p.His172= | |
| XM_005256321.4:c.516C>T | XP_005256378.1:p.His172= | |
| XM_006721264.4:c.516C>T | XP_006721327.1:p.His172= | |
| XM_017023597.1:c.516C>T | XP_016879086.1:p.His172= | |
| XM_017023598.1:c.516C>T | XP_016879087.1:p.His172= | |
| XR_001751971.2:n.555C>T | ||
| XR_001751972.2:n.555C>T | ||
| NM_003119.4:c.516C>T MANE Select | NP_003110.1:p.His172= | |
| NM_199367.3:c.516C>T | NP_955399.1:p.His172= |