Linked Data
gnomAD v4:
1-204190413-C-CCCCA
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204190413_204190414insCCCA , CM000663.2:g.204190413_204190414insCCCA | GRCh38 |
| NC_000001.10:g.204159541_204159542insCCCA , CM000663.1:g.204159541_204159542insCCCA | GRCh37 |
| NC_000001.9:g.202426164_202426165insCCCA | NCBI36 |
| NG_032151.1:g.11078_11079insTGGG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367194.5:c.*70_*71insTGGG MANE Select | ENSP00000356162.4:n.*70_*71insTGGG | |
| ENST00000367194.4:c.*70_*71insTGGG | ENSP00000356162.4:n.*70_*71insTGGG | |
| NM_002256.3:c.*70_*71insTGGG | NP_002247.3:n.*70_*71insTGGG | |
| XM_011509525.1:c.*70_*71insTGGG | XP_011507827.1:n.*70_*71insTGGG | |
| NM_002256.4:c.*70_*71insTGGG MANE Select | NP_002247.3:n.*70_*71insTGGG |