Linked Data
dbSNP Id:
rs148320917
MyVariant Identifiers:
chr6:g.31370396_31370397insGGGGGG (hg19)
chr6:g.31402619_31402620insGGGGGG (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31402620_31402621insGGGGGG , CM000668.2:g.31402620_31402621insGGGGGG | GRCh38 |
| NC_000006.11:g.31370397_31370398insGGGGGG , CM000668.1:g.31370397_31370398insGGGGGG | GRCh37 |
| NC_000006.10:g.31478376_31478377insGGGGGG | NCBI36 |
| NG_034139.1:g.7837_7838insGGGGGG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000667609.1:n.528_529insGGGGGG | ||
| ENST00000673647.1:c.-189+264_-189+265insGGGGGG | ENSP00000500967.1:n.-189+264_-189+265insGGGGGG | |
| ENST00000673996.1:n.79+1837_79+1838insGGGGGG | ||
| ENST00000674069.1:c.-173+1857_-173+1858insGGGGGG | ENSP00000501157.1:n.-173+1857_-173+1858insGGGGGG | |
| ENST00000674131.1:c.-189+264_-189+265insGGGGGG | ENSP00000501002.1:n.-189+264_-189+265insGGGGGG | |
| ENST00000616296.4:c.-222+1837_-222+1838insGGGGGG | ENSP00000482382.1:n.-222+1837_-222+1838insGGGGGG | |
| NM_001289152.1:c.-222+1837_-222+1838insGGGGGG | NP_001276081.1:n.-222+1837_-222+1838insGGGGGG | |
| NM_001289153.1:c.-222+1857_-222+1858insGGGGGG | NP_001276082.1:n.-222+1857_-222+1858insGGGGGG | |
| NM_001289154.1:c.-173+1857_-173+1858insGGGGGG | NP_001276083.1:n.-173+1857_-173+1858insGGGGGG | |
| NM_001289152.2:c.-222+1837_-222+1838insGGGGGG | NP_001276081.1:n.-222+1837_-222+1838insGGGGGG | |
| NM_001289153.2:c.-222+1857_-222+1858insGGGGGG | NP_001276082.1:n.-222+1857_-222+1858insGGGGGG | |
| NM_001289154.2:c.-173+1857_-173+1858insGGGGGG | NP_001276083.1:n.-173+1857_-173+1858insGGGGGG |