Linked Data
ClinVar Variation Id:
472788
dbSNP Id:
rs780868977
ExAC:
9:130242262 G / A
gnomAD v2:
9-130242262-G-A
gnomAD v3:
9-127479983-G-A
gnomAD v4:
9-127479983-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.127479983G>A , CM000671.2:g.127479983G>A | GRCh38 |
| NC_000009.11:g.130242262G>A , CM000671.1:g.130242262G>A | GRCh37 |
| NC_000009.10:g.129282083G>A | NCBI36 |
| NG_032008.1:g.33498G>A , LRG_373:g.33498G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000300417.11:c.1043+5G>A MANE Select | ENSP00000300417.6:n.1043+5G>A | |
| ENST00000472068.2:c.*766+5G>A | ENSP00000501555.1:n.*766+5G>A | |
| ENST00000498513.6:c.296+5G>A | ENSP00000501637.1:n.296+5G>A | |
| ENST00000674511.1:n.918+5G>A | ||
| ENST00000674516.1:c.1043+5G>A | ENSP00000502441.1:n.1043+5G>A | |
| ENST00000674621.1:n.949+5G>A | ||
| ENST00000674771.1:c.1043+5G>A | ENSP00000502627.1:n.1043+5G>A | |
| ENST00000674784.1:c.*273+5G>A | ENSP00000501837.1:n.*273+5G>A | |
| ENST00000674970.1:c.*817+5G>A | ENSP00000502493.1:n.*817+5G>A | |
| ENST00000675012.1:n.923+5G>A | ||
| ENST00000675141.1:c.1043+5G>A | ENSP00000502420.1:n.1043+5G>A | |
| ENST00000675198.1:n.945+5G>A | ||
| ENST00000675213.1:c.998+5G>A | ENSP00000502218.1:n.998+5G>A | |
| ENST00000675224.1:c.1043+5G>A | ENSP00000501869.1:n.1043+5G>A | |
| ENST00000675253.1:c.1043+5G>A | ENSP00000502557.1:n.1043+5G>A | |
| ENST00000675445.1:c.*715+5G>A | ENSP00000502253.1:n.*715+5G>A | |
| ENST00000675448.1:c.1043+5G>A | ENSP00000502167.1:n.1043+5G>A | |
| ENST00000675521.1:n.895+5G>A | ||
| ENST00000675572.1:c.1043+5G>A | ENSP00000501598.1:n.1043+5G>A | |
| ENST00000675641.1:c.1043+5G>A | ENSP00000501845.1:n.1043+5G>A | |
| ENST00000675657.1:c.1043+5G>A | ENSP00000502002.1:n.1043+5G>A | |
| ENST00000675662.1:n.936+5G>A | ||
| ENST00000675789.1:c.1043+5G>A | ENSP00000501954.1:n.1043+5G>A | |
| ENST00000675883.1:c.1043+5G>A | ENSP00000501592.1:n.1043+5G>A | |
| ENST00000675945.1:c.1043+5G>A | ENSP00000501835.1:n.1043+5G>A | |
| ENST00000676014.1:c.986+5G>A | ENSP00000502058.1:n.986+5G>A | |
| ENST00000676035.1:n.804+5G>A | ||
| ENST00000676106.1:n.848+5G>A | ||
| ENST00000676137.1:n.934+5G>A | ||
| ENST00000676170.1:c.1043+5G>A | ENSP00000502177.1:n.1043+5G>A | |
| ENST00000676318.1:c.1043+5G>A | ENSP00000502300.1:n.1043+5G>A | |
| ENST00000676336.1:c.821+5G>A | ENSP00000502686.1:n.821+5G>A | |
| ENST00000676349.1:c.*812+5G>A | ENSP00000502155.1:n.*812+5G>A | |
| ENST00000676399.1:n.941+5G>A | ||
| ENST00000676409.1:n.922+5G>A | ||
| ENST00000300417.10:c.1043+5G>A | ENSP00000300417.6:n.1043+5G>A | |
| ENST00000323301.8:c.1043+5G>A | ENSP00000322937.4:n.1043+5G>A | |
| ENST00000373322.1:c.1043+5G>A | ENSP00000362419.1:n.1043+5G>A | |
| ENST00000373324.8:c.1043+5G>A | ENSP00000362421.4:n.1043+5G>A | |
| ENST00000472068.1:n.30+5G>A | ||
| ENST00000483302.5:n.260+5G>A | ||
| ENST00000498513.5:n.296+5G>A | ||
| NM_001005373.3:c.1043+5G>A | NP_001005373.1:n.1043+5G>A | |
| NM_001005374.3:c.1043+5G>A | NP_001005374.1:n.1043+5G>A | |
| NM_001190723.2:c.1043+5G>A | NP_001177652.1:n.1043+5G>A | |
| NM_138361.5:c.1043+5G>A , LRG_373t1:c.1043+5G>A | NP_612370.3:n.1043+5G>A | |
| XM_006717316.2:c.1043+5G>A | XP_006717379.1:n.1043+5G>A | |
| XR_929874.1:n.1415+5G>A | ||
| XM_006717316.4:c.1043+5G>A | XP_006717379.1:n.1043+5G>A | |
| XM_017015283.1:c.1043+5G>A | XP_016870772.1:n.1043+5G>A | |
| XM_017015284.2:c.254+5G>A | XP_016870773.1:n.254+5G>A | |
| XR_001746415.2:n.1397+5G>A | ||
| XR_929874.3:n.1397+5G>A | ||
| NM_001190723.3:c.1043+5G>A | NP_001177652.1:n.1043+5G>A | |
| NM_001005373.4:c.1043+5G>A MANE Select | NP_001005373.1:n.1043+5G>A | |
| NM_001005374.4:c.1043+5G>A | NP_001005374.1:n.1043+5G>A | |
| NM_001384142.1:c.1043+5G>A | NP_001371071.1:n.1043+5G>A | |
| NM_001384143.1:c.1043+5G>A | NP_001371072.1:n.1043+5G>A | |
| NM_001384144.1:c.254+5G>A | NP_001371073.1:n.254+5G>A | |
| NR_168891.1:n.1391+5G>A | ||
| NR_168892.1:n.1391+5G>A |