Linked Data
dbSNP Id:
rs765424797
ExAC:
10:96058123 T / C
gnomAD v2:
10-96058123-T-C
gnomAD v4:
10-94298366-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94298366T>C , CM000672.2:g.94298366T>C | GRCh38 |
| NC_000010.10:g.96058123T>C , CM000672.1:g.96058123T>C | GRCh37 |
| NC_000010.9:g.96048113T>C | NCBI36 |
| NG_015799.1:g.309378T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000371375.2:c.4244-13T>C | ENSP00000360426.1:n.4244-13T>C | |
| ENST00000685253.1:c.*1711-13T>C | ENSP00000509405.1:n.*1711-13T>C | |
| ENST00000685889.1:n.1903-13T>C | ||
| ENST00000686807.1:n.587-13T>C | ||
| ENST00000686954.1:c.*452-13T>C | ENSP00000508416.1:n.*452-13T>C | |
| ENST00000688810.1:c.4196-13T>C | ENSP00000509140.1:n.4196-13T>C | |
| ENST00000689233.1:n.9376-13T>C | ||
| ENST00000690340.1:n.2841-13T>C | ||
| ENST00000692286.1:c.5036-13T>C | ENSP00000509490.1:n.5036-13T>C | |
| ENST00000692396.1:c.5120-13T>C | ENSP00000508605.1:n.5120-13T>C | |
| ENST00000371380.8:c.5168-13T>C MANE Select | ENSP00000360431.2:n.5168-13T>C | |
| ENST00000371385.8:c.4142-13T>C | ENSP00000360438.4:n.4142-13T>C | |
| ENST00000674738.1:c.3723-13T>C | ||
| ENST00000674827.1:c.3284-13T>C | ENSP00000502523.1:n.3284-13T>C | |
| ENST00000675218.1:c.4244-13T>C | ENSP00000501910.1:n.4244-13T>C | |
| ENST00000675487.1:c.*1101-13T>C | ENSP00000502340.1:n.*1101-13T>C | |
| ENST00000675718.1:c.4437-13T>C | ||
| ENST00000676102.1:c.4013-13T>C | ENSP00000502811.1:n.4013-13T>C | |
| ENST00000260766.7:c.5168-13T>C | ENSP00000260766.3:n.5168-13T>C | |
| ENST00000371375.1:c.4244-13T>C | ENSP00000360426.1:n.4244-13T>C | |
| ENST00000371380.7:c.5168-13T>C | ENSP00000360431.2:n.5168-13T>C | |
| ENST00000371385.7:c.4244-13T>C | ENSP00000360438.3:n.4244-13T>C | |
| NM_001165979.2:c.4244-13T>C | NP_001159451.1:n.4244-13T>C | |
| NM_001288989.1:c.5120-13T>C | NP_001275918.1:n.5120-13T>C | |
| NM_016341.3:c.5168-13T>C | NP_057425.3:n.5168-13T>C | |
| XM_006717885.2:c.5210-13T>C | XP_006717948.1:n.5210-13T>C | |
| XM_006717886.2:c.5210-13T>C | XP_006717949.1:n.5210-13T>C | |
| XM_006717888.2:c.5207-13T>C | XP_006717951.1:n.5207-13T>C | |
| XM_006717889.2:c.5162-13T>C | XP_006717952.1:n.5162-13T>C | |
| XM_006717890.1:c.4286-13T>C | XP_006717953.1:n.4286-13T>C | |
| XM_011539849.1:c.5210-13T>C | XP_011538151.1:n.5210-13T>C | |
| XM_011539850.1:c.4055-13T>C | XP_011538152.1:n.4055-13T>C | |
| XM_006717885.4:c.5210-13T>C | XP_006717948.1:n.5210-13T>C | |
| XM_006717888.4:c.5207-13T>C | XP_006717951.1:n.5207-13T>C | |
| XM_006717889.4:c.5162-13T>C | XP_006717952.1:n.5162-13T>C | |
| XM_006717890.3:c.4286-13T>C | XP_006717953.1:n.4286-13T>C | |
| XM_011539849.3:c.5210-13T>C | XP_011538151.1:n.5210-13T>C | |
| XM_011539850.3:c.4055-13T>C | XP_011538152.1:n.4055-13T>C | |
| XM_017016310.2:c.5210-13T>C | XP_016871799.1:n.5210-13T>C | |
| XM_017016311.2:c.5210-13T>C | XP_016871800.1:n.5210-13T>C | |
| XM_017016312.2:c.4196-13T>C | XP_016871801.1:n.4196-13T>C | |
| NM_001288989.2:c.5120-13T>C | NP_001275918.1:n.5120-13T>C | |
| NM_016341.4:c.5168-13T>C MANE Select | NP_057425.3:n.5168-13T>C |