Linked Data
gnomAD v4:
11-67583616-C-CT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.67583616_67583617insT , CM000673.2:g.67583616_67583617insT | GRCh38 |
| NC_000011.9:g.67351087_67351088insT , CM000673.1:g.67351087_67351088insT | GRCh37 |
| NC_000011.8:g.67107663_67107664insT | NCBI36 |
| NG_012075.1:g.5022_5023insT , LRG_723:g.5022_5023insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000398606.7:c.-228_-227insT | ENSP00000381607.3:n.-228_-227insT | |
| NM_000852.3:c.-228_-227insT , LRG_723t1:c.-228_-227insT | NP_000843.1:n.-228_-227insT |