Linked Data
gnomAD v4:
22-50578944-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.50578944C>T , CM000684.2:g.50578944C>T | GRCh38 |
| NC_000022.10:g.51017373C>T , CM000684.1:g.51017373C>T | GRCh37 |
| NC_000022.9:g.49364239C>T | NCBI36 |
| NG_012643.1:g.4724G>A | |
| NG_029213.1:g.9056G>A , LRG_855:g.9056G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000452668.1:n.319+92G>A | ||
| ENST00000453634.5:c.328+92G>A | ENSP00000457031.1:n.328+92G>A | |
| ENST00000492556.5:n.2189+92G>A | ||
| NR_027928.2:n.1551+92G>A |