Linked Data
dbSNP Id:
rs1744964863
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.185969008_185969009insGG , CM000665.2:g.185969008_185969009insGG | GRCh38 |
| NC_000003.11:g.185686797_185686798insGG , CM000665.1:g.185686797_185686798insGG | GRCh37 |
| NC_000003.10:g.187169491_187169492insGG | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000306399.3:n.270+300_270+301insGG | ||
| ENST00000416764.5:n.349+291_349+292insGG | ||
| ENST00000422108.5:n.288+359_288+360insGG | ||
| ENST00000423298.5:n.137-2607_137-2606insGG | ||
| ENST00000436375.5:n.342+300_342+301insGG | ||
| ENST00000445507.1:n.279+359_279+360insGG | ||
| NR_033752.2:n.349+291_349+292insGG | ||
| NR_151491.1:n.137-2607_137-2606insGG |