Linked Data
gnomAD v4:
4-68646934-C-CT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.68646934_68646935insT , CM000666.2:g.68646934_68646935insT | GRCh38 |
| NC_000004.11:g.69512652_69512653insT , CM000666.1:g.69512652_69512653insT | GRCh37 |
| NC_000004.10:g.69195247_69195248insT | NCBI36 |
| NG_052676.1:g.28842_28843insA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000338206.6:c.*169_*170insA MANE Select | ENSP00000341045.5:n.*169_*170insA | |
| ENST00000338206.5:c.*169_*170insA | ENSP00000341045.5:n.*169_*170insA | |
| ENST00000616841.4:c.1732+30_1732+31insA | ENSP00000482004.1:n.1732+30_1732+31insA | |
| NM_001076.3:c.*169_*170insA | NP_001067.2:n.*169_*170insA | |
| NM_001076.4:c.*169_*170insA MANE Select | NP_001067.2:n.*169_*170insA |