Linked Data
ClinVar Variation Id:
191155
dbSNP Id:
rs786205550
gnomAD v2:
2-233635714-A-G
gnomAD v3:
2-232771004-A-G
gnomAD v4:
2-232771004-A-G
PubMed:
PMID:25475713
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232771004A>G , CM000664.2:g.232771004A>G | GRCh38 |
| NC_000002.11:g.233635714A>G , CM000664.1:g.233635714A>G | GRCh37 |
| NC_000002.10:g.233343958A>G | NCBI36 |
| NG_011847.1:g.78700A>G | |
| NG_016742.1:g.10562T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233826.4:c.359T>C (KCNJ13) MANE Select | ENSP00000233826.3:p.Ile120Thr | |
| ENST00000373563.9:c.532+9568A>G (GIGYF2) MANE Select | ENSP00000362664.5:n.532+9568A>G | |
| ENST00000424038.2:c.*137+9568A>G (GIGYF2) | ENSP00000399064.1:n.*137+9568A>G | |
| ENST00000677450.1:c.13+2599A>G (GIGYF2) | ENSP00000503420.1:n.13+2599A>G | |
| ENST00000677591.1:c.-195+6394A>G (GIGYF2) | ENSP00000503061.1:n.-195+6394A>G | |
| ENST00000678230.1:c.25+5025A>G (GIGYF2) | ENSP00000504272.1:n.25+5025A>G | |
| ENST00000678339.1:c.-213+6394A>G (GIGYF2) | ENSP00000503437.1:n.-213+6394A>G | |
| ENST00000678466.1:c.-213+2745A>G (GIGYF2) | ENSP00000504219.1:n.-213+2745A>G | |
| ENST00000233826.3:c.359T>C (KCNJ13) | ENSP00000233826.3:p.Ile120Thr | |
| ENST00000373563.8:c.532+9568A>G (GIGYF2) | ENSP00000362664.4:n.532+9568A>G | |
| ENST00000409196.7:c.532+9568A>G (GIGYF2) | ENSP00000387070.3:n.532+9568A>G | |
| ENST00000409451.7:c.533-5408A>G (GIGYF2) | ENSP00000387170.3:n.533-5408A>G | |
| ENST00000409480.5:c.533-5408A>G (GIGYF2) | ENSP00000386765.1:n.533-5408A>G | |
| ENST00000409547.5:c.532+9568A>G (GIGYF2) | ENSP00000386537.1:n.532+9568A>G | |
| ENST00000409779.1:c.224+135T>C (KCNJ13) | ENSP00000386408.1:n.224+135T>C | |
| ENST00000410029.1:c.359T>C (KCNJ13) | ENSP00000386251.1:p.Ile120Thr | |
| ENST00000421778.1:c.13+2599A>G (GIGYF2) | ENSP00000390325.1:n.13+2599A>G | |
| ENST00000423659.5:c.379+14670A>G (GIGYF2) | ENSP00000404195.1:n.379+14670A>G | |
| ENST00000424038.1:c.*137+9568A>G (GIGYF2) | ENSP00000399064.1:n.*137+9568A>G | |
| ENST00000424414.6:c.-195+6394A>G (GIGYF2) | ENSP00000401261.2:n.-195+6394A>G | |
| ENST00000436349.5:c.-213+6394A>G (GIGYF2) | ENSP00000400076.1:n.-213+6394A>G | |
| ENST00000438786.1:c.119T>C (KCNJ13) | ENSP00000407284.1:p.Ile40Thr | |
| ENST00000440945.5:c.532+9568A>G (GIGYF2) | ENSP00000410297.1:n.532+9568A>G | |
| ENST00000444142.1:c.261T>C (KCNJ13) | ||
| ENST00000445650.5:c.25+5025A>G (GIGYF2) | ENSP00000392218.1:n.25+5025A>G | |
| ENST00000455139.5:c.-213+2745A>G (GIGYF2) | ENSP00000395299.1:n.-213+2745A>G | |
| ENST00000463554.5:n.685-20A>G (GIGYF2) | ||
| ENST00000629305.2:c.533-5408A>G (GIGYF2) | ENSP00000487548.1:n.533-5408A>G | |
| NM_001103146.1:c.532+9568A>G (GIGYF2) | NP_001096616.1:n.532+9568A>G | |
| NM_001103147.1:c.533-5408A>G (GIGYF2) | NP_001096617.1:n.533-5408A>G | |
| NM_001103148.1:c.532+9568A>G (GIGYF2) | NP_001096618.1:n.532+9568A>G | |
| NM_001172416.1:c.224+135T>C (KCNJ13) | NP_001165887.1:n.224+135T>C | |
| NM_001172417.1:c.119T>C (KCNJ13) | NP_001165888.1:p.Ile40Thr | |
| NM_002242.4:c.359T>C (KCNJ13) MANE Select | NP_002233.2:p.Ile120Thr | |
| NM_015575.3:c.532+9568A>G (GIGYF2) | NP_056390.2:n.532+9568A>G | |
| NR_103492.1:n.645+9568A>G (GIGYF2) | ||
| NM_001103146.3:c.532+9568A>G (GIGYF2) MANE Select | NP_001096616.1:n.532+9568A>G | |
| NM_001103147.2:c.533-5408A>G (GIGYF2) | NP_001096617.1:n.533-5408A>G | |
| NM_001103148.2:c.532+9568A>G (GIGYF2) | NP_001096618.1:n.532+9568A>G | |
| NM_015575.4:c.532+9568A>G (GIGYF2) | NP_056390.2:n.532+9568A>G |