Linked Data
ClinVar Variation Id:
335045
ClinVar RCV Id:
RCV000379488
dbSNP Id:
rs886055794
gnomAD v4:
2-232767849-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.232767849T>C , CM000664.2:g.232767849T>C | GRCh38 |
| NC_000002.11:g.233632559T>C , CM000664.1:g.233632559T>C | GRCh37 |
| NC_000002.10:g.233340803T>C | NCBI36 |
| NG_011847.1:g.75545T>C | |
| NG_016742.1:g.13717A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233826.4:c.*342A>G (KCNJ13) MANE Select | ENSP00000233826.3:n.*342A>G | |
| ENST00000373563.9:c.532+6413T>C (GIGYF2) MANE Select | ENSP00000362664.5:n.532+6413T>C | |
| ENST00000424038.2:c.*137+6413T>C (GIGYF2) | ENSP00000399064.1:n.*137+6413T>C | |
| ENST00000677591.1:c.-195+3239T>C (GIGYF2) | ENSP00000503061.1:n.-195+3239T>C | |
| ENST00000678230.1:c.25+1870T>C (GIGYF2) | ENSP00000504272.1:n.25+1870T>C | |
| ENST00000678339.1:c.-213+3239T>C (GIGYF2) | ENSP00000503437.1:n.-213+3239T>C | |
| ENST00000233826.3:c.*342A>G (KCNJ13) | ENSP00000233826.3:n.*342A>G | |
| ENST00000373563.8:c.532+6413T>C (GIGYF2) | ENSP00000362664.4:n.532+6413T>C | |
| ENST00000409196.7:c.532+6413T>C (GIGYF2) | ENSP00000387070.3:n.532+6413T>C | |
| ENST00000409451.7:c.532+6413T>C (GIGYF2) | ENSP00000387170.3:n.532+6413T>C | |
| ENST00000409480.5:c.532+6413T>C (GIGYF2) | ENSP00000386765.1:n.532+6413T>C | |
| ENST00000409547.5:c.532+6413T>C (GIGYF2) | ENSP00000386537.1:n.532+6413T>C | |
| ENST00000423659.5:c.379+11515T>C (GIGYF2) | ENSP00000404195.1:n.379+11515T>C | |
| ENST00000424038.1:c.*137+6413T>C (GIGYF2) | ENSP00000399064.1:n.*137+6413T>C | |
| ENST00000424414.6:c.-195+3239T>C (GIGYF2) | ENSP00000401261.2:n.-195+3239T>C | |
| ENST00000436349.5:c.-213+3239T>C (GIGYF2) | ENSP00000400076.1:n.-213+3239T>C | |
| ENST00000440945.5:c.532+6413T>C (GIGYF2) | ENSP00000410297.1:n.532+6413T>C | |
| ENST00000445650.5:c.25+1870T>C (GIGYF2) | ENSP00000392218.1:n.25+1870T>C | |
| ENST00000463554.5:n.685-3175T>C (GIGYF2) | ||
| ENST00000473170.5:n.436-411T>C (GIGYF2) | ||
| ENST00000475530.1:n.150-411T>C (GIGYF2) | ||
| ENST00000629305.2:c.532+6413T>C (GIGYF2) | ENSP00000487548.1:n.532+6413T>C | |
| NM_001103146.1:c.532+6413T>C (GIGYF2) | NP_001096616.1:n.532+6413T>C | |
| NM_001103147.1:c.532+6413T>C (GIGYF2) | NP_001096617.1:n.532+6413T>C | |
| NM_001103148.1:c.532+6413T>C (GIGYF2) | NP_001096618.1:n.532+6413T>C | |
| NM_001172416.1:c.*904A>G (KCNJ13) | NP_001165887.1:n.*904A>G | |
| NM_001172417.1:c.*342A>G (KCNJ13) | NP_001165888.1:n.*342A>G | |
| NM_002242.4:c.*342A>G (KCNJ13) MANE Select | NP_002233.2:n.*342A>G | |
| NM_015575.3:c.532+6413T>C (GIGYF2) | NP_056390.2:n.532+6413T>C | |
| NR_103492.1:n.645+6413T>C (GIGYF2) | ||
| NM_001103146.3:c.532+6413T>C (GIGYF2) MANE Select | NP_001096616.1:n.532+6413T>C | |
| NM_001103147.2:c.532+6413T>C (GIGYF2) | NP_001096617.1:n.532+6413T>C | |
| NM_001103148.2:c.532+6413T>C (GIGYF2) | NP_001096618.1:n.532+6413T>C | |
| NM_015575.4:c.532+6413T>C (GIGYF2) | NP_056390.2:n.532+6413T>C |