Linked Data
dbSNP Id:
rs1212548203
gnomAD v2:
16-2134743-T-C
gnomAD v3:
16-2084742-T-C
gnomAD v4:
16-2084742-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.2084742T>C , CM000678.2:g.2084742T>C | GRCh38 |
| NC_000016.9:g.2134743T>C , CM000678.1:g.2134743T>C | GRCh37 |
| NC_000016.8:g.2074744T>C | NCBI36 |
| NG_005895.1:g.40437T>C , LRG_487:g.40437T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000568566.6:c.*2842+27T>C | ENSP00000455997.2:n.*2842+27T>C | |
| ENST00000642206.2:c.4340+27T>C | ENSP00000495146.2:n.4340+27T>C | |
| ENST00000642365.2:c.4490+27T>C | ENSP00000495459.2:n.4490+27T>C | |
| ENST00000644417.2:c.*4873+27T>C | ENSP00000493912.2:n.*4873+27T>C | |
| ENST00000646464.2:c.*7242+27T>C | ENSP00000496610.2:n.*7242+27T>C | |
| ENST00000219476.9:c.4493+27T>C MANE Select | ENSP00000219476.3:n.4493+27T>C | |
| ENST00000350773.9:c.4424+27T>C | ENSP00000344383.4:n.4424+27T>C | |
| ENST00000401874.7:c.4292+27T>C | ENSP00000384468.2:n.4292+27T>C | |
| ENST00000568454.6:c.4325+27T>C | ENSP00000454487.1:n.4325+27T>C | |
| ENST00000569110.2:c.716+40T>C | ||
| ENST00000569930.2:n.2375+27T>C | ||
| ENST00000642365.1:c.3147+27T>C | ||
| ENST00000642561.1:c.4364+27T>C | ENSP00000495099.1:n.4364+27T>C | |
| ENST00000642728.1:n.675+27T>C | ||
| ENST00000642797.1:c.4295+27T>C | ENSP00000493846.1:n.4295+27T>C | |
| ENST00000642936.1:c.4361+27T>C | ENSP00000494514.1:n.4361+27T>C | |
| ENST00000643088.1:c.4292+27T>C | ENSP00000494747.1:n.4292+27T>C | |
| ENST00000643177.1:n.507+27T>C | ||
| ENST00000643426.1:n.2141+27T>C | ||
| ENST00000643946.1:c.4424+27T>C | ENSP00000495927.1:n.4424+27T>C | |
| ENST00000644043.1:c.4364+27T>C | ENSP00000496262.1:n.4364+27T>C | |
| ENST00000644329.1:c.4292+27T>C | ENSP00000496611.1:n.4292+27T>C | |
| ENST00000644335.1:c.4295+27T>C | ENSP00000496317.1:n.4295+27T>C | |
| ENST00000644399.1:c.4414+27T>C | ||
| ENST00000645024.1:n.2577+27T>C | ||
| ENST00000646388.1:c.4493+27T>C | ENSP00000495921.1:n.4493+27T>C | |
| ENST00000646634.1:n.3308+27T>C | ||
| ENST00000646674.1:n.1745+27T>C | ||
| ENST00000647042.1:n.1716+27T>C | ||
| ENST00000647180.1:n.1606+27T>C | ||
| ENST00000219476.7:c.4493+27T>C | ENSP00000219476.3:n.4493+27T>C | |
| ENST00000350773.8:c.4424+27T>C | ENSP00000344383.4:n.4424+27T>C | |
| ENST00000382538.10:c.4148+27T>C | ENSP00000371978.6:n.4148+27T>C | |
| ENST00000401874.6:c.4292+27T>C | ENSP00000384468.2:n.4292+27T>C | |
| ENST00000439117.6:c.*3660+27T>C | ENSP00000406980.2:n.*3660+27T>C | |
| ENST00000439673.6:c.4184+27T>C | ENSP00000399232.2:n.4184+27T>C | |
| ENST00000497886.5:n.2251+27T>C | ||
| ENST00000568454.5:c.4325+27T>C | ENSP00000454487.1:n.4325+27T>C | |
| ENST00000569110.1:c.675+27T>C | ||
| ENST00000569930.1:n.1608+27T>C | ||
| NM_000548.3:c.4493+27T>C , LRG_487t1:c.4493+27T>C | NP_000539.2:n.4493+27T>C | |
| NM_001077183.1:c.4292+27T>C | NP_001070651.1:n.4292+27T>C | |
| NM_001114382.1:c.4424+27T>C | NP_001107854.1:n.4424+27T>C | |
| XM_005255529.3:c.4364+27T>C | XP_005255586.2:n.4364+27T>C | |
| XM_005255531.3:c.4295+27T>C | XP_005255588.2:n.4295+27T>C | |
| XM_011522636.1:c.4547+27T>C | XP_011520938.1:n.4547+27T>C | |
| XM_011522637.1:c.4544+27T>C | XP_011520939.1:n.4544+27T>C | |
| XM_011522638.1:c.4436+27T>C | XP_011520940.1:n.4436+27T>C | |
| XM_011522639.1:c.4418+27T>C | XP_011520941.1:n.4418+27T>C | |
| XM_011522640.1:c.4415+27T>C | XP_011520942.1:n.4415+27T>C | |
| XM_011522641.1:c.4184+27T>C | XP_011520943.1:n.4184+27T>C | |
| NM_000548.4:c.4493+27T>C | NP_000539.2:n.4493+27T>C | |
| NM_001077183.2:c.4292+27T>C | NP_001070651.1:n.4292+27T>C | |
| NM_001114382.2:c.4424+27T>C | NP_001107854.1:n.4424+27T>C | |
| NM_001318827.1:c.4184+27T>C | NP_001305756.1:n.4184+27T>C | |
| NM_001318829.1:c.4148+27T>C | NP_001305758.1:n.4148+27T>C | |
| NM_001318831.1:c.3761+27T>C | NP_001305760.1:n.3761+27T>C | |
| NM_001318832.1:c.4325+27T>C | NP_001305761.1:n.4325+27T>C | |
| NM_001363528.1:c.4295+27T>C | NP_001350457.1:n.4295+27T>C | |
| NM_021055.2:c.4364+27T>C | NP_066399.2:n.4364+27T>C | |
| XM_005255531.4:c.4295+27T>C | XP_005255588.2:n.4295+27T>C | |
| XM_011522636.2:c.4547+27T>C | XP_011520938.1:n.4547+27T>C | |
| XM_011522637.2:c.4544+27T>C | XP_011520939.1:n.4544+27T>C | |
| XM_011522638.2:c.4709+27T>C | XP_011520940.2:n.4709+27T>C | |
| XM_011522639.2:c.4418+27T>C | XP_011520941.1:n.4418+27T>C | |
| XM_011522640.2:c.4415+27T>C | XP_011520942.1:n.4415+27T>C | |
| XM_017023615.1:c.4490+27T>C | XP_016879104.1:n.4490+27T>C | |
| XM_017023616.1:c.4361+27T>C | XP_016879105.1:n.4361+27T>C | |
| XM_017023617.1:c.4457+27T>C | XP_016879106.1:n.4457+27T>C | |
| XM_017023618.1:c.3203+27T>C | XP_016879107.1:n.3203+27T>C | |
| XM_024450413.1:c.4292+27T>C | XP_024306181.1:n.4292+27T>C | |
| NM_000548.5:c.4493+27T>C MANE Select | NP_000539.2:n.4493+27T>C | |
| NM_001370404.1:c.4361+27T>C | NP_001357333.1:n.4361+27T>C | |
| NM_001370405.1:c.4364+27T>C | NP_001357334.1:n.4364+27T>C | |
| NM_001077183.3:c.4292+27T>C | NP_001070651.1:n.4292+27T>C | |
| NM_001114382.3:c.4424+27T>C | NP_001107854.1:n.4424+27T>C | |
| NM_001318827.2:c.4184+27T>C | NP_001305756.1:n.4184+27T>C | |
| NM_001318829.2:c.4148+27T>C | NP_001305758.1:n.4148+27T>C | |
| NM_001318831.2:c.3761+27T>C | NP_001305760.1:n.3761+27T>C | |
| NM_001318832.2:c.4325+27T>C | NP_001305761.1:n.4325+27T>C | |
| NM_001363528.2:c.4295+27T>C | NP_001350457.1:n.4295+27T>C | |
| NM_021055.3:c.4364+27T>C | NP_066399.2:n.4364+27T>C |