Linked Data
gnomAD v4:
3-150926160-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.150926160A>C , CM000665.2:g.150926160A>C | GRCh38 |
| NC_000003.11:g.150643947A>C , CM000665.1:g.150643947A>C | GRCh37 |
| NC_000003.10:g.152126637A>C | NCBI36 |
| NG_009168.1:g.51840T>G , LRG_700:g.51840T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000562308.5:c.104+15422T>G | ||
| ENST00000565169.1:c.162+15422T>G | ||
| ENST00000569170.5:c.162+15422T>G | ||
| XR_924167.1:n.2787T>G |