Linked Data
ClinVar Variation Id:
411682
dbSNP Id:
rs746053679
ExAC:
16:89579446 G / T
gnomAD v2:
16-89579446-G-T
gnomAD v3:
16-89513038-G-T
gnomAD v4:
16-89513038-G-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89513038G>T , CM000678.2:g.89513038G>T | GRCh38 |
| NC_000016.9:g.89579446G>T , CM000678.1:g.89579446G>T | GRCh37 |
| NC_000016.8:g.88106947G>T | NCBI36 |
| NG_008082.1:g.9642G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000268704.7:c.376+1G>T | ENSP00000268704.3:n.376+1G>T | |
| ENST00000562775.2:n.240+1G>T | ||
| ENST00000564047.2:n.385+1G>T | ||
| ENST00000564409.2:c.145+1G>T | ENSP00000495297.1:n.145+1G>T | |
| ENST00000566371.6:c.376+1G>T | ENSP00000454475.2:n.376+1G>T | |
| ENST00000569363.2:n.391+1G>T | ||
| ENST00000642334.1:c.249+1G>T | ||
| ENST00000642371.1:c.308+1G>T | ||
| ENST00000642436.1:n.388+1G>T | ||
| ENST00000643105.1:c.296+1G>T | ||
| ENST00000643178.1:n.24+1G>T | ||
| ENST00000643307.1:c.376+1G>T | ENSP00000495673.1:n.376+1G>T | |
| ENST00000643345.1:c.376+1G>T | ENSP00000493982.1:n.376+1G>T | |
| ENST00000643649.1:c.376+1G>T | ENSP00000494806.1:n.376+1G>T | |
| ENST00000643668.1:c.376+1G>T | ENSP00000494903.1:n.376+1G>T | |
| ENST00000643724.1:c.376+1G>T | ENSP00000496335.1:n.376+1G>T | |
| ENST00000643954.1:c.114+1G>T | ||
| ENST00000643957.1:c.259+1G>T | ENSP00000494246.1:n.259+1G>T | |
| ENST00000644210.1:c.376+1G>T | ENSP00000495675.1:n.376+1G>T | |
| ENST00000644225.1:n.393+1G>T | ||
| ENST00000644498.1:c.376+1G>T | ENSP00000496244.1:n.376+1G>T | |
| ENST00000644671.1:c.39+1G>T | ||
| ENST00000644781.1:c.376+1G>T | ENSP00000495473.1:n.376+1G>T | |
| ENST00000644901.1:c.376+1G>T | ENSP00000493797.1:n.376+1G>T | |
| ENST00000645042.1:c.376+1G>T | ENSP00000493908.1:n.376+1G>T | |
| ENST00000645063.1:c.376+1G>T | ENSP00000493590.1:n.376+1G>T | |
| ENST00000645354.1:c.291+1G>T | ||
| ENST00000645533.1:c.376+1G>T | ENSP00000495690.1:n.376+1G>T | |
| ENST00000645818.2:c.376+1G>T MANE Select | ENSP00000495795.2:n.376+1G>T | |
| ENST00000645897.1:c.376+1G>T | ENSP00000495293.1:n.376+1G>T | |
| ENST00000645977.1:n.391+1G>T | ||
| ENST00000646263.1:c.376+1G>T | ENSP00000494119.1:n.376+1G>T | |
| ENST00000646303.1:c.244+1G>T | ENSP00000494160.1:n.244+1G>T | |
| ENST00000646399.1:c.59+1G>T | ||
| ENST00000646445.1:c.182+1G>T | ||
| ENST00000646531.1:c.376+1G>T | ENSP00000495185.1:n.376+1G>T | |
| ENST00000646589.1:c.376+1G>T | ENSP00000494739.1:n.376+1G>T | |
| ENST00000646716.1:c.376+1G>T | ENSP00000495593.1:n.376+1G>T | |
| ENST00000646826.1:c.376+1G>T | ENSP00000495123.1:n.376+1G>T | |
| ENST00000646930.1:c.376+1G>T | ENSP00000495219.1:n.376+1G>T | |
| ENST00000646958.1:n.326+1G>T | ||
| ENST00000647079.1:c.-33+1G>T | ENSP00000495967.1:n.-33+1G>T | |
| ENST00000647227.1:c.139+1G>T | ||
| ENST00000268704.6:c.376+1G>T | ENSP00000268704.2:n.376+1G>T | |
| ENST00000341316.6:c.376+1G>T | ENSP00000341157.2:n.376+1G>T | |
| ENST00000566371.5:c.244+1G>T | ENSP00000454475.1:n.244+1G>T | |
| ENST00000568151.1:c.472+1G>T | ENSP00000457719.1:n.472+1G>T | |
| ENST00000569363.1:n.217+1G>T | ||
| ENST00000620811.4:c.-1201+1G>T | ENSP00000478030.1:n.-1201+1G>T | |
| NM_003119.3:c.376+1G>T | NP_003110.1:n.376+1G>T | |
| NM_199367.2:c.376+1G>T | NP_955399.1:n.376+1G>T | |
| XM_005256321.3:c.376+1G>T | XP_005256378.1:n.376+1G>T | |
| XM_006721264.2:c.376+1G>T | XP_006721327.1:n.376+1G>T | |
| XM_011523306.1:c.376+1G>T | XP_011521608.1:n.376+1G>T | |
| XM_011523307.1:c.376+1G>T | XP_011521609.1:n.376+1G>T | |
| NM_001363850.1:c.376+1G>T | NP_001350779.1:n.376+1G>T | |
| XM_005256321.4:c.376+1G>T | XP_005256378.1:n.376+1G>T | |
| XM_006721264.4:c.376+1G>T | XP_006721327.1:n.376+1G>T | |
| XM_017023597.1:c.376+1G>T | XP_016879086.1:n.376+1G>T | |
| XM_017023598.1:c.376+1G>T | XP_016879087.1:n.376+1G>T | |
| XR_001751971.2:n.415+1G>T | ||
| XR_001751972.2:n.415+1G>T | ||
| NM_003119.4:c.376+1G>T MANE Select | NP_003110.1:n.376+1G>T | |
| NM_199367.3:c.376+1G>T | NP_955399.1:n.376+1G>T |