Linked Data
gnomAD v4:
1-204190416-C-CCG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.204190417_204190418insGC , CM000663.2:g.204190417_204190418insGC | GRCh38 |
| NC_000001.10:g.204159545_204159546insGC , CM000663.1:g.204159545_204159546insGC | GRCh37 |
| NC_000001.9:g.202426168_202426169insGC | NCBI36 |
| NG_032151.1:g.11075_11076insCG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367194.5:c.*67_*68insCG MANE Select | ENSP00000356162.4:n.*67_*68insCG | |
| ENST00000367194.4:c.*67_*68insCG | ENSP00000356162.4:n.*67_*68insCG | |
| NM_002256.3:c.*67_*68insCG | NP_002247.3:n.*67_*68insCG | |
| XM_011509525.1:c.*67_*68insCG | XP_011507827.1:n.*67_*68insCG | |
| NM_002256.4:c.*67_*68insCG MANE Select | NP_002247.3:n.*67_*68insCG |