Linked Data
gnomAD v4:
3-150926190-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.150926190T>C , CM000665.2:g.150926190T>C | GRCh38 |
| NC_000003.11:g.150643977T>C , CM000665.1:g.150643977T>C | GRCh37 |
| NC_000003.10:g.152126667T>C | NCBI36 |
| NG_009168.1:g.51810A>G , LRG_700:g.51810A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295911.6:c.*662A>G | ENSP00000295911.2:n.*662A>G | |
| ENST00000562308.5:c.104+15392A>G | ||
| ENST00000565169.1:c.162+15392A>G | ||
| ENST00000569170.5:c.162+15392A>G | ||
| NM_052995.2:c.*662A>G , LRG_700t2:c.*662A>G | NP_443721.1:n.*662A>G | |
| XR_924167.1:n.2757A>G |