Linked Data
ClinVar Variation Id:
236034
ClinVar RCV Id:
RCV000225059
dbSNP Id:
rs878853225
MyVariant Identifiers:
chr6:g.76568710_76568712delinsC (hg19)
chr6:g.75858993_75858995delinsC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.75858993_75858995delinsC , CM000668.2:g.75858993_75858995delinsC | GRCh38 |
| NC_000006.11:g.76568710_76568712delinsC , CM000668.1:g.76568710_76568712delinsC | GRCh37 |
| NC_000006.10:g.76625430_76625432delinsC | NCBI36 |
| NG_009934.1:g.114802_114804delinsC | |
| NG_009934.2:g.114801_114803delinsC |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000369975.6:c.1473_1473+2delinsC | ||
| ENST00000369977.8:c.1473_1473+2delinsC | ||
| ENST00000369985.9:c.1473_1473+2delinsC | ||
| ENST00000462633.3:c.*1029_*1029+2delinsC | ||
| ENST00000627432.3:c.1482_1482+2delinsC | ||
| ENST00000653423.1:c.1473_1473+2delinsC | ||
| ENST00000653917.1:c.1482_1482+2delinsC | ||
| ENST00000660420.1:c.*1429_*1429+2delinsC | ||
| ENST00000662184.1:c.1392_1392+2delinsC | ||
| ENST00000662603.1:c.1473_1473+2delinsC | ||
| ENST00000663400.1:c.1473_1473+2delinsC | ||
| ENST00000664209.1:c.1473_1473+2delinsC | ||
| ENST00000664640.1:c.1473_1473+2delinsC | ||
| ENST00000671923.1:c.1473_1473+2delinsC | ||
| ENST00000672093.1:c.1473_1473+2delinsC | ||
| ENST00000369975.5:c.1473_1473+2delinsC | ||
| ENST00000369977.7:c.1473_1473+2delinsC | ||
| ENST00000369981.7:c.1473_1473+2delinsC | ||
| ENST00000369985.8:c.1473_1473+2delinsC | ||
| ENST00000615563.4:c.1473_1473+2delinsC | ||
| ENST00000627432.2:c.1473_1473+2delinsC | ||
| NM_001300899.1:c.1473_1473+2delinsC | ||
| NM_004999.3:c.1473_1473+2delinsC | ||
| XM_005248719.2:c.1473_1473+2delinsC | ||
| XM_005248720.2:c.1473_1473+2delinsC | ||
| XM_005248721.2:c.1473_1473+2delinsC | ||
| XM_005248722.2:c.1473_1473+2delinsC | ||
| XM_005248724.2:c.1473_1473+2delinsC | ||
| XM_005248726.2:c.1473_1473+2delinsC | ||
| XM_005248719.4:c.1473_1473+2delinsC | ||
| XM_005248720.4:c.1473_1473+2delinsC | ||
| XM_005248721.4:c.1473_1473+2delinsC | ||
| XM_005248722.4:c.1473_1473+2delinsC | ||
| XM_005248724.4:c.1473_1473+2delinsC | ||
| XM_005248726.4:c.1473_1473+2delinsC | ||
| XM_017010899.2:c.1473_1473+2delinsC | ||
| XM_024446447.1:c.1473_1473+2delinsC | ||
| XM_024446448.1:c.1473_1473+2delinsC | ||
| NM_004999.4:c.1473_1473+2delinsC | ||
| NM_001300899.2:c.1473_1473+2delinsC | ||
| NM_001368136.1:c.1473_1473+2delinsC | ||
| NM_001368137.1:c.1473_1473+2delinsC | ||
| NM_001368138.1:c.1458_1458+2delinsC | ||
| NM_001368865.1:c.1473_1473+2delinsC | ||
| NM_001368866.1:c.1473_1473+2delinsC | ||
| NR_160538.1:n.1705_1705+2delinsC |