Linked Data
gnomAD v4:
1-204190397-C-CG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204190397_204190398insG , CM000663.2:g.204190397_204190398insG | GRCh38 |
| NC_000001.10:g.204159525_204159526insG , CM000663.1:g.204159525_204159526insG | GRCh37 |
| NC_000001.9:g.202426148_202426149insG | NCBI36 |
| NG_032151.1:g.11094_11095insC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367194.5:c.*86_*87insC MANE Select | ENSP00000356162.4:n.*86_*87insC | |
| ENST00000367194.4:c.*86_*87insC | ENSP00000356162.4:n.*86_*87insC | |
| NM_002256.3:c.*86_*87insC | NP_002247.3:n.*86_*87insC | |
| XM_011509525.1:c.*86_*87insC | XP_011507827.1:n.*86_*87insC | |
| NM_002256.4:c.*86_*87insC MANE Select | NP_002247.3:n.*86_*87insC |