Linked Data
dbSNP Id:
rs1554758225
gnomAD v2:
9-136136997-G-GGGA
gnomAD v3:
9-133261594-G-GGGA
gnomAD v4:
9-133261594-G-GGGA
MyVariant Identifiers:
chr9:g.136136997_136136998insGGA (hg19)
chr9:g.133261594_133261595insGGA (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133261594_133261595insGGA , CM000671.2:g.133261594_133261595insGGA | GRCh38 |
| NC_000009.11:g.136136997_136136998insGGA , CM000671.1:g.136136997_136136998insGGA | GRCh37 |
| NC_000009.10:g.135126818_135126819insGGA | NCBI36 |
| NG_006669.1:g.16055_16056insTCC | |
| NG_006669.2:g.18620_18621insTCC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000453660.4:n.129-221_129-220insTCC | ||
| ENST00000647353.1:n.54-10443_54-10442insTCC | ||
| ENST00000651471.1:n.134-221_134-220insTCC | ||
| ENST00000679909.1:c.28+13567_28+13568insTCC | ENSP00000506089.1:n.28+13567_28+13568insTCC | |
| ENST00000453660.3:n.111-221_111-220insTCC | ||
| ENST00000538324.2:c.99-221_99-220insTCC | ENSP00000483018.1:n.99-221_99-220insTCC | |
| ENST00000611156.4:c.99-221_99-220insTCC | ENSP00000483265.1:n.99-221_99-220insTCC | |
| NM_020469.2:c.99-221_99-220insTCC | NP_065202.2:n.99-221_99-220insTCC | |
| NM_020469.3:c.99-221_99-220insTCC | NP_065202.2:n.99-221_99-220insTCC |