Linked Data
gnomAD v4:
4-68646933-T-TG
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.68646933_68646934insG , CM000666.2:g.68646933_68646934insG | GRCh38 |
| NC_000004.11:g.69512651_69512652insG , CM000666.1:g.69512651_69512652insG | GRCh37 |
| NC_000004.10:g.69195246_69195247insG | NCBI36 |
| NG_052676.1:g.28843_28844insC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338206.6:c.*170_*171insC MANE Select | ENSP00000341045.5:n.*170_*171insC | |
| ENST00000338206.5:c.*170_*171insC | ENSP00000341045.5:n.*170_*171insC | |
| ENST00000616841.4:c.1732+31_1732+32insC | ENSP00000482004.1:n.1732+31_1732+32insC | |
| NM_001076.3:c.*170_*171insC | NP_001067.2:n.*170_*171insC | |
| NM_001076.4:c.*170_*171insC MANE Select | NP_001067.2:n.*170_*171insC |