Linked Data
dbSNP Id:
rs11187837
gnomAD v2:
10-96035980-T-C
gnomAD v3:
10-94276223-T-C
gnomAD v4:
10-94276223-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.94276223T>C , CM000672.2:g.94276223T>C | GRCh38 |
| NC_000010.10:g.96035980T>C , CM000672.1:g.96035980T>C | GRCh37 |
| NC_000010.9:g.96025970T>C | NCBI36 |
| NG_015799.1:g.287235T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000371375.2:c.3741+2503T>C | ENSP00000360426.1:n.3741+2503T>C | |
| ENST00000685253.1:c.*1208+2503T>C | ENSP00000509405.1:n.*1208+2503T>C | |
| ENST00000685889.1:n.1400+2503T>C | ||
| ENST00000686954.1:c.4665+2503T>C | ENSP00000508416.1:n.4665+2503T>C | |
| ENST00000688810.1:c.3693+2503T>C | ENSP00000509140.1:n.3693+2503T>C | |
| ENST00000689233.1:n.4995+2503T>C | ||
| ENST00000692286.1:c.4665+2503T>C | ENSP00000509490.1:n.4665+2503T>C | |
| ENST00000692396.1:c.4617+2503T>C | ENSP00000508605.1:n.4617+2503T>C | |
| ENST00000371380.8:c.4665+2503T>C MANE Select | ENSP00000360431.2:n.4665+2503T>C | |
| ENST00000371385.8:c.3639+2503T>C | ENSP00000360438.4:n.3639+2503T>C | |
| ENST00000674738.1:c.3070+2503T>C | ||
| ENST00000674827.1:c.2742+2503T>C | ENSP00000502523.1:n.2742+2503T>C | |
| ENST00000675218.1:c.3741+2503T>C | ENSP00000501910.1:n.3741+2503T>C | |
| ENST00000675487.1:c.*598+2503T>C | ENSP00000502340.1:n.*598+2503T>C | |
| ENST00000675718.1:c.3892+2503T>C | ||
| ENST00000676102.1:c.3510+2503T>C | ENSP00000502811.1:n.3510+2503T>C | |
| ENST00000260766.7:c.4665+2503T>C | ENSP00000260766.3:n.4665+2503T>C | |
| ENST00000371375.1:c.3741+2503T>C | ENSP00000360426.1:n.3741+2503T>C | |
| ENST00000371380.7:c.4665+2503T>C | ENSP00000360431.2:n.4665+2503T>C | |
| ENST00000371385.7:c.3741+2503T>C | ENSP00000360438.3:n.3741+2503T>C | |
| NM_001165979.2:c.3741+2503T>C | NP_001159451.1:n.3741+2503T>C | |
| NM_001288989.1:c.4617+2503T>C | NP_001275918.1:n.4617+2503T>C | |
| NM_016341.3:c.4665+2503T>C | NP_057425.3:n.4665+2503T>C | |
| XM_006717885.2:c.4665+2503T>C | XP_006717948.1:n.4665+2503T>C | |
| XM_006717886.2:c.4665+2503T>C | XP_006717949.1:n.4665+2503T>C | |
| XM_006717888.2:c.4665+2503T>C | XP_006717951.1:n.4665+2503T>C | |
| XM_006717889.2:c.4617+2503T>C | XP_006717952.1:n.4617+2503T>C | |
| XM_006717890.1:c.3741+2503T>C | XP_006717953.1:n.3741+2503T>C | |
| XM_011539849.1:c.4665+2503T>C | XP_011538151.1:n.4665+2503T>C | |
| XM_011539850.1:c.3510+2503T>C | XP_011538152.1:n.3510+2503T>C | |
| XM_011539851.1:c.4665+2503T>C | XP_011538153.1:n.4665+2503T>C | |
| XM_011539852.1:c.4665+2503T>C | XP_011538154.1:n.4665+2503T>C | |
| XM_006717885.4:c.4665+2503T>C | XP_006717948.1:n.4665+2503T>C | |
| XM_006717888.4:c.4665+2503T>C | XP_006717951.1:n.4665+2503T>C | |
| XM_006717889.4:c.4617+2503T>C | XP_006717952.1:n.4617+2503T>C | |
| XM_006717890.3:c.3741+2503T>C | XP_006717953.1:n.3741+2503T>C | |
| XM_011539849.3:c.4665+2503T>C | XP_011538151.1:n.4665+2503T>C | |
| XM_011539850.3:c.3510+2503T>C | XP_011538152.1:n.3510+2503T>C | |
| XM_011539851.3:c.4665+2503T>C | XP_011538153.1:n.4665+2503T>C | |
| XM_011539852.3:c.4665+2503T>C | XP_011538154.1:n.4665+2503T>C | |
| XM_017016310.2:c.4665+2503T>C | XP_016871799.1:n.4665+2503T>C | |
| XM_017016311.2:c.4665+2503T>C | XP_016871800.1:n.4665+2503T>C | |
| XM_017016312.2:c.3693+2503T>C | XP_016871801.1:n.3693+2503T>C | |
| NM_001288989.2:c.4617+2503T>C | NP_001275918.1:n.4617+2503T>C | |
| NM_016341.4:c.4665+2503T>C MANE Select | NP_057425.3:n.4665+2503T>C |