Linked Data
ClinVar Variation Id:
64868
dbSNP Id:
rs45490993
ExAC:
16:2137891 G / A
gnomAD v2:
16-2137891-G-A
gnomAD v3:
16-2087890-G-A
gnomAD v4:
16-2087890-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2087890G>A , CM000678.2:g.2087890G>A | GRCh38 |
| NC_000016.9:g.2137891G>A , CM000678.1:g.2137891G>A | GRCh37 |
| NC_000016.8:g.2077892G>A | NCBI36 |
| NG_005895.1:g.43585G>A , LRG_487:g.43585G>A | |
| NG_008617.1:g.55331C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.*3366G>A | ENSP00000455997.2:n.*3366G>A | |
| ENST00000642206.2:c.4864G>A | ENSP00000495146.2:p.Val1622Ile | |
| ENST00000642365.2:c.5014G>A | ENSP00000495459.2:p.Val1672Ile | |
| ENST00000644417.2:c.*5530G>A | ENSP00000493912.2:n.*5530G>A | |
| ENST00000646464.2:c.*7766G>A | ENSP00000496610.2:n.*7766G>A | |
| ENST00000219476.9:c.5017G>A MANE Select | ENSP00000219476.3:p.Val1673Ile | |
| ENST00000350773.9:c.4948G>A | ENSP00000344383.4:p.Val1650Ile | |
| ENST00000401874.7:c.4816G>A | ENSP00000384468.2:p.Val1606Ile | |
| ENST00000568454.6:c.4849G>A | ENSP00000454487.1:p.Val1617Ile | |
| ENST00000569110.2:c.1240G>A | ||
| ENST00000569930.2:n.2899G>A | ||
| ENST00000642365.1:c.3671G>A | ||
| ENST00000642561.1:c.4888G>A | ENSP00000495099.1:p.Val1630Ile | |
| ENST00000642791.1:n.614G>A | ||
| ENST00000642797.1:c.4819G>A | ENSP00000493846.1:p.Val1607Ile | |
| ENST00000642936.1:c.4885G>A | ENSP00000494514.1:p.Val1629Ile | |
| ENST00000643088.1:c.4810G>A | ENSP00000494747.1:p.Val1604Ile | |
| ENST00000643177.1:n.1031G>A | ||
| ENST00000643426.1:n.2665G>A | ||
| ENST00000643946.1:c.4942G>A | ENSP00000495927.1:p.Val1648Ile | |
| ENST00000644043.1:c.4888G>A | ENSP00000496262.1:p.Val1630Ile | |
| ENST00000644278.1:n.499G>A | ||
| ENST00000644329.1:c.4816G>A | ENSP00000496611.1:p.Val1606Ile | |
| ENST00000644335.1:c.4813G>A | ENSP00000496317.1:p.Val1605Ile | |
| ENST00000644399.1:c.4938G>A | ||
| ENST00000645024.1:n.3101G>A | ||
| ENST00000646388.1:c.5011G>A | ENSP00000495921.1:p.Val1671Ile | |
| ENST00000646634.1:n.3832G>A | ||
| ENST00000646674.1:n.2269G>A | ||
| ENST00000647042.1:n.2240G>A | ||
| ENST00000647180.1:n.2130G>A | ||
| ENST00000219476.7:c.5017G>A | ENSP00000219476.3:p.Val1673Ile | |
| ENST00000350773.8:c.4948G>A | ENSP00000344383.4:p.Val1650Ile | |
| ENST00000382538.10:c.4672G>A | ENSP00000371978.6:p.Val1558Ile | |
| ENST00000401874.6:c.4816G>A | ENSP00000384468.2:p.Val1606Ile | |
| ENST00000439117.6:c.*4184G>A | ENSP00000406980.2:n.*4184G>A | |
| ENST00000439673.6:c.4708G>A | ENSP00000399232.2:p.Val1570Ile | |
| ENST00000497886.5:n.2740G>A | ||
| ENST00000568454.5:c.4849G>A | ENSP00000454487.1:p.Val1617Ile | |
| ENST00000569110.1:c.1199G>A | ||
| ENST00000569930.1:n.2132G>A | ||
| NM_000548.3:c.5017G>A , LRG_487t1:c.5017G>A | NP_000539.2:p.Val1673Ile | |
| NM_001077183.1:c.4816G>A | NP_001070651.1:p.Val1606Ile | |
| NM_001114382.1:c.4948G>A | NP_001107854.1:p.Val1650Ile | |
| XM_005255529.3:c.4888G>A | XP_005255586.2:p.Val1630Ile | |
| XM_005255531.3:c.4819G>A | XP_005255588.2:p.Val1607Ile | |
| XM_011522636.1:c.5071G>A | XP_011520938.1:p.Val1691Ile | |
| XM_011522637.1:c.5068G>A | XP_011520939.1:p.Val1690Ile | |
| XM_011522638.1:c.4960G>A | XP_011520940.1:p.Val1654Ile | |
| XM_011522639.1:c.4942G>A | XP_011520941.1:p.Val1648Ile | |
| XM_011522640.1:c.4939G>A | XP_011520942.1:p.Val1647Ile | |
| XM_011522641.1:c.4708G>A | XP_011520943.1:p.Val1570Ile | |
| NM_000548.4:c.5017G>A | NP_000539.2:p.Val1673Ile | |
| NM_001077183.2:c.4816G>A | NP_001070651.1:p.Val1606Ile | |
| NM_001114382.2:c.4948G>A | NP_001107854.1:p.Val1650Ile | |
| NM_001318827.1:c.4708G>A | NP_001305756.1:p.Val1570Ile | |
| NM_001318829.1:c.4672G>A | NP_001305758.1:p.Val1558Ile | |
| NM_001318831.1:c.4285G>A | NP_001305760.1:p.Val1429Ile | |
| NM_001318832.1:c.4849G>A | NP_001305761.1:p.Val1617Ile | |
| NM_001363528.1:c.4819G>A | NP_001350457.1:p.Val1607Ile | |
| NM_021055.2:c.4888G>A | NP_066399.2:p.Val1630Ile | |
| XM_005255531.4:c.4819G>A | XP_005255588.2:p.Val1607Ile | |
| XM_011522636.2:c.5071G>A | XP_011520938.1:p.Val1691Ile | |
| XM_011522637.2:c.5068G>A | XP_011520939.1:p.Val1690Ile | |
| XM_011522638.2:c.5233G>A | XP_011520940.2:p.Val1745Ile | |
| XM_011522639.2:c.4942G>A | XP_011520941.1:p.Val1648Ile | |
| XM_011522640.2:c.4939G>A | XP_011520942.1:p.Val1647Ile | |
| XM_017023615.1:c.5014G>A | XP_016879104.1:p.Val1672Ile | |
| XM_017023616.1:c.4885G>A | XP_016879105.1:p.Val1629Ile | |
| XM_017023617.1:c.4981G>A | XP_016879106.1:p.Val1661Ile | |
| XM_017023618.1:c.3727G>A | XP_016879107.1:p.Val1243Ile | |
| XM_024450413.1:c.4816G>A | XP_024306181.1:p.Val1606Ile | |
| NM_000548.5:c.5017G>A MANE Select | NP_000539.2:p.Val1673Ile | |
| NM_001370404.1:c.4885G>A | NP_001357333.1:p.Val1629Ile | |
| NM_001370405.1:c.4888G>A | NP_001357334.1:p.Val1630Ile | |
| NM_001077183.3:c.4816G>A | NP_001070651.1:p.Val1606Ile | |
| NM_001114382.3:c.4948G>A | NP_001107854.1:p.Val1650Ile | |
| NM_001318827.2:c.4708G>A | NP_001305756.1:p.Val1570Ile | |
| NM_001318829.2:c.4672G>A | NP_001305758.1:p.Val1558Ile | |
| NM_001318831.2:c.4285G>A | NP_001305760.1:p.Val1429Ile | |
| NM_001318832.2:c.4849G>A | NP_001305761.1:p.Val1617Ile | |
| NM_001363528.2:c.4819G>A | NP_001350457.1:p.Val1607Ile | |
| NM_021055.3:c.4888G>A | NP_066399.2:p.Val1630Ile |