Linked Data
gnomAD v4:
2-43887320-GC-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.43887322del , CM000664.2:g.43887322del | GRCh38 |
| NC_000002.11:g.44114461del , CM000664.1:g.44114461del | GRCh37 |
| NC_000002.10:g.43967965del | NCBI36 |
| NG_008247.1:g.113685del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000682612.1:c.2231del | ||
| ENST00000684454.1:n.9328del | ||
| ENST00000260665.12:c.*1279del MANE Select | ENSP00000260665.7:n.*1279del | |
| ENST00000260665.11:c.*1279del | ENSP00000260665.7:n.*1279del | |
| NM_133259.3:c.*1279del | NP_573566.2:n.*1279del | |
| XR_002958896.1:n.5646del | ||
| NM_133259.4:c.*1279del MANE Select | NP_573566.2:n.*1279del |