Linked Data
ClinVar Variation Id:
486631
dbSNP Id:
rs1555441265
gnomAD v3:
16-2088491-C-T
gnomAD v4:
16-2088491-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2088491C>T , CM000678.2:g.2088491C>T | GRCh38 |
| NC_000016.9:g.2138492C>T , CM000678.1:g.2138492C>T | GRCh37 |
| NC_000016.8:g.2078493C>T | NCBI36 |
| NG_005895.1:g.44186C>T , LRG_487:g.44186C>T | |
| NG_008617.1:g.54730G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000568566.6:c.*3654C>T | ENSP00000455997.2:n.*3654C>T | |
| ENST00000642206.2:c.5152C>T | ENSP00000495146.2:p.His1718Tyr | |
| ENST00000642365.2:c.5302C>T | ENSP00000495459.2:p.His1768Tyr | |
| ENST00000644417.2:c.*5818C>T | ENSP00000493912.2:n.*5818C>T | |
| ENST00000646464.2:c.*8054C>T | ENSP00000496610.2:n.*8054C>T | |
| ENST00000219476.9:c.5305C>T MANE Select | ENSP00000219476.3:p.His1769Tyr | |
| ENST00000350773.9:c.5236C>T | ENSP00000344383.4:p.His1746Tyr | |
| ENST00000401874.7:c.5104C>T | ENSP00000384468.2:p.His1702Tyr | |
| ENST00000568454.6:c.5137C>T | ENSP00000454487.1:p.His1713Tyr | |
| ENST00000569110.2:c.1528C>T | ||
| ENST00000569930.2:n.3187C>T | ||
| ENST00000642365.1:c.3959C>T | ||
| ENST00000642561.1:c.5164C>T | ENSP00000495099.1:p.His1722Tyr | |
| ENST00000642791.1:n.902C>T | ||
| ENST00000642797.1:c.5107C>T | ENSP00000493846.1:p.His1703Tyr | |
| ENST00000642936.1:c.5173C>T | ENSP00000494514.1:p.His1725Tyr | |
| ENST00000643088.1:c.5098C>T | ENSP00000494747.1:p.His1700Tyr | |
| ENST00000643426.1:n.2953C>T | ||
| ENST00000643946.1:c.5230C>T | ENSP00000495927.1:p.His1744Tyr | |
| ENST00000644043.1:c.5176C>T | ENSP00000496262.1:p.His1726Tyr | |
| ENST00000644329.1:c.5191C>T | ENSP00000496611.1:p.His1731Tyr | |
| ENST00000644335.1:c.5101C>T | ENSP00000496317.1:p.His1701Tyr | |
| ENST00000644399.1:c.5226C>T | ||
| ENST00000645024.1:n.3389C>T | ||
| ENST00000646388.1:c.5299C>T | ENSP00000495921.1:p.His1767Tyr | |
| ENST00000646634.1:n.4120C>T | ||
| ENST00000646674.1:n.2557C>T | ||
| ENST00000647042.1:n.2528C>T | ||
| ENST00000647180.1:n.2418C>T | ||
| ENST00000219476.7:c.5305C>T | ENSP00000219476.3:p.His1769Tyr | |
| ENST00000350773.8:c.5236C>T | ENSP00000344383.4:p.His1746Tyr | |
| ENST00000382538.10:c.4960C>T | ENSP00000371978.6:p.His1654Tyr | |
| ENST00000401874.6:c.5104C>T | ENSP00000384468.2:p.His1702Tyr | |
| ENST00000439117.6:c.*4472C>T | ENSP00000406980.2:n.*4472C>T | |
| ENST00000439673.6:c.4996C>T | ENSP00000399232.2:p.His1666Tyr | |
| ENST00000497886.5:n.3028C>T | ||
| ENST00000568454.5:c.5137C>T | ENSP00000454487.1:p.His1713Tyr | |
| ENST00000569110.1:c.1487C>T | ||
| ENST00000569930.1:n.2420C>T | ||
| NM_000548.3:c.5305C>T , LRG_487t1:c.5305C>T | NP_000539.2:p.His1769Tyr | |
| NM_001077183.1:c.5104C>T | NP_001070651.1:p.His1702Tyr | |
| NM_001114382.1:c.5236C>T | NP_001107854.1:p.His1746Tyr | |
| XM_005255529.3:c.5176C>T | XP_005255586.2:p.His1726Tyr | |
| XM_005255531.3:c.5107C>T | XP_005255588.2:p.His1703Tyr | |
| XM_011522636.1:c.5359C>T | XP_011520938.1:p.His1787Tyr | |
| XM_011522637.1:c.5356C>T | XP_011520939.1:p.His1786Tyr | |
| XM_011522638.1:c.5248C>T | XP_011520940.1:p.His1750Tyr | |
| XM_011522639.1:c.5230C>T | XP_011520941.1:p.His1744Tyr | |
| XM_011522640.1:c.5227C>T | XP_011520942.1:p.His1743Tyr | |
| XM_011522641.1:c.4996C>T | XP_011520943.1:p.His1666Tyr | |
| NM_000548.4:c.5305C>T | NP_000539.2:p.His1769Tyr | |
| NM_001077183.2:c.5104C>T | NP_001070651.1:p.His1702Tyr | |
| NM_001114382.2:c.5236C>T | NP_001107854.1:p.His1746Tyr | |
| NM_001318827.1:c.4996C>T | NP_001305756.1:p.His1666Tyr | |
| NM_001318829.1:c.4960C>T | NP_001305758.1:p.His1654Tyr | |
| NM_001318831.1:c.4573C>T | NP_001305760.1:p.His1525Tyr | |
| NM_001318832.1:c.5137C>T | NP_001305761.1:p.His1713Tyr | |
| NM_001363528.1:c.5107C>T | NP_001350457.1:p.His1703Tyr | |
| NM_021055.2:c.5176C>T | NP_066399.2:p.His1726Tyr | |
| XM_005255531.4:c.5107C>T | XP_005255588.2:p.His1703Tyr | |
| XM_011522636.2:c.5359C>T | XP_011520938.1:p.His1787Tyr | |
| XM_011522637.2:c.5356C>T | XP_011520939.1:p.His1786Tyr | |
| XM_011522638.2:c.5521C>T | XP_011520940.2:p.His1841Tyr | |
| XM_011522639.2:c.5230C>T | XP_011520941.1:p.His1744Tyr | |
| XM_011522640.2:c.5227C>T | XP_011520942.1:p.His1743Tyr | |
| XM_017023615.1:c.5302C>T | XP_016879104.1:p.His1768Tyr | |
| XM_017023616.1:c.5173C>T | XP_016879105.1:p.His1725Tyr | |
| XM_017023617.1:c.5269C>T | XP_016879106.1:p.His1757Tyr | |
| XM_017023618.1:c.4015C>T | XP_016879107.1:p.His1339Tyr | |
| XM_024450413.1:c.5191C>T | XP_024306181.1:p.His1731Tyr | |
| NM_000548.5:c.5305C>T MANE Select | NP_000539.2:p.His1769Tyr | |
| NM_001370404.1:c.5173C>T | NP_001357333.1:p.His1725Tyr | |
| NM_001370405.1:c.5164C>T | NP_001357334.1:p.His1722Tyr | |
| NM_001077183.3:c.5104C>T | NP_001070651.1:p.His1702Tyr | |
| NM_001114382.3:c.5236C>T | NP_001107854.1:p.His1746Tyr | |
| NM_001318827.2:c.4996C>T | NP_001305756.1:p.His1666Tyr | |
| NM_001318829.2:c.4960C>T | NP_001305758.1:p.His1654Tyr | |
| NM_001318831.2:c.4573C>T | NP_001305760.1:p.His1525Tyr | |
| NM_001318832.2:c.5137C>T | NP_001305761.1:p.His1713Tyr | |
| NM_001363528.2:c.5107C>T | NP_001350457.1:p.His1703Tyr | |
| NM_021055.3:c.5176C>T | NP_066399.2:p.His1726Tyr |